http://identifiers.org/exac.variant/19-14499350-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499350
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499350
    reference: chr 19
allele count: 370
allele frequency: 5.904883498244494e-3
allele num: 62660
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.73+38C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.73+38C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.167+38C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.73+38C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.73+38C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.232+38C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.73+38C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.73+38C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-164C>A
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 1.75e1
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 2.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 9196
  bin: 2.25e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13592
  bin: 1.25e1
  variant carriers: 137
genotype depth: GenotypeDepth
  all individuals: 23791
  bin: 7.5e0
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 2.5e0
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 27055
  bin: 2.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 3829
  bin: 3.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 5.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 9.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 3670
  bin: 2.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 2.5e0
  variant carriers: 4
num of homozygotes: 4
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

19-14499354-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499354
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499354
    reference: chr 19
allele count: 1
allele frequency: 1.528724737823707e-5
allele num: 65414
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.73+42G>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.232+42G>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.73+42G>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-160G>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.73+42G>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.73+42G>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.73+42G>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.73+42G>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.167+42G>T
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12409
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23096
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3831
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3273
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1008
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4510
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum

19-14499355-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499355
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499355
    reference: chr 19
allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.73+43C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.73+43C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-159C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.232+43C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.73+43C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.73+43C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.73+43C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.73+43C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.167+43C>G
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12611
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3635
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12055
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4257
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 933
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum

19-14499357-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499357
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499357
    reference: chr 19
allele count: 74698
allele frequency: 8.828924662553483e-1
allele num: 84606
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.167+45T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.73+45T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.73+45T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.73+45T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.73+45T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-157T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.73+45T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.73+45T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.232+45T>A
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 9.75e1
  variant carriers: 509
genotype depth: GenotypeDepth
  all individuals: 13272
  bin: 1.75e1
  variant carriers: 13263
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 3.75e1
  variant carriers: 1820
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.75e1
  variant carriers: 188
genotype depth: GenotypeDepth
  all individuals: 10823
  bin: 2.25e1
  variant carriers: 10816
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.25e1
  variant carriers: 874
genotype depth: GenotypeDepth
  all individuals: 6745
  bin: 2.75e1
  variant carriers: 6742
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 2.5e0
  variant carriers: 1213
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.25e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.75e1
  variant carriers: 501
genotype depth: GenotypeDepth
  all individuals: 11696
  bin: 1.25e1
  variant carriers: 11662
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 125
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 322
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 146
genotype depth: GenotypeDepth
  all individuals: 7211
  bin: 7.5e0
  variant carriers: 7120
genotype depth: GenotypeDepth
  all individuals: 3712
  bin: 3.25e1
  variant carriers: 3712
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 179
genotype quality: GenotypeQuality
  all individuals: 3204
  bin: 1.25e1
  variant carriers: 3204
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 8.25e1
  variant carriers: 1361
genotype quality: GenotypeQuality
  all individuals: 3942
  bin: 4.75e1
  variant carriers: 3941
genotype quality: GenotypeQuality
  all individuals: 1218
  bin: 7.25e1
  variant carriers: 1218
genotype quality: GenotypeQuality
  all individuals: 3264
  bin: 7.5e0
  variant carriers: 3233
genotype quality: GenotypeQuality
  all individuals: 1635
  bin: 7.75e1
  variant carriers: 1635
num of homozygotes: 32417
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

19-14499361-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499361
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499361
    reference: chr 19
allele count: 1
allele frequency: 9.752482006670697e-6
allele num: 102538
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.73+49G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.73+49G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-153G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.232+49G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.73+49G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.167+49G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.73+49G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.73+49G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.73+49G>A
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7033
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11726
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11916
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5297
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2167
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1033
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5057
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2388
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

19-14499463-T-TTG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499463
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499465
    reference: chr 19
allele count: 1
allele frequency: 8.260776182530111e-6
allele num: 121054
alternate allele: TTG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.74-47_74-46dupGT
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.74-47_74-46dupGT
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.233-47_233-46dupGT
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.74-47_74-46dupGT
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.74-47_74-46dupGT
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.168-47_168-46dupGT
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-47_23-46dupGT
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.74-47_74-46dupGT
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.74-47_74-46dupGT
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40361
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

19-14499467-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499467
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499467
    reference: chr 19
allele count: 7
allele frequency: 5.783594421310067e-5
allele num: 121032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.74-47G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.74-47G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.74-47G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-47G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.74-47G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.74-47G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.74-47G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.233-47G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.168-47G>A
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40361
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-14499468-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499468
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499468
    reference: chr 19
allele count: 7220
allele frequency: 5.985541849051598e-2
allele num: 120624
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.168-46T>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.74-46T>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.74-46T>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-46T>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.74-46T>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.233-46T>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.74-46T>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.74-46T>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.74-46T>G
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 6.25e1
  variant carriers: 200
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 2.25e1
  variant carriers: 227
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 4.75e1
  variant carriers: 174
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 8.25e1
  variant carriers: 379
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.25e1
  variant carriers: 224
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 9.25e1
  variant carriers: 401
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 7.75e1
  variant carriers: 345
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 3.75e1
  variant carriers: 194
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 275
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 244
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 1.75e1
  variant carriers: 155
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 3.25e1
  variant carriers: 245
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 2.75e1
  variant carriers: 241
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.75e1
  variant carriers: 209
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 40634
  bin: 9.75e1
  variant carriers: 2856
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.25e1
  variant carriers: 196
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 8.75e1
  variant carriers: 409
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 2.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 52311
  bin: 9.75e1
  variant carriers: 6789
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 1248
  bin: 6.75e1
  variant carriers: 20
num of homozygotes: 205
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

19-14499471-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499471
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499471
    reference: chr 19
allele count: 7228
allele frequency: 5.986417094583402e-2
allele num: 120740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.74-43T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.74-43T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.74-43T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.74-43T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-43T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.233-43T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.74-43T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.168-43T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.74-43T>C
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41032
  bin: 9.75e1
  variant carriers: 3253
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 6.75e1
  variant carriers: 211
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 2.75e1
  variant carriers: 241
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 3.25e1
  variant carriers: 240
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 9.25e1
  variant carriers: 394
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.75e1
  variant carriers: 180
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 1.75e1
  variant carriers: 149
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 8.75e1
  variant carriers: 328
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.25e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 3.75e1
  variant carriers: 189
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 8.25e1
  variant carriers: 354
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.75e1
  variant carriers: 180
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.25e1
  variant carriers: 197
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 2.25e1
  variant carriers: 201
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 7.75e1
  variant carriers: 262
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 7.25e1
  variant carriers: 246
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 164
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 3.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 4.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 3.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 2.25e1
  variant carriers: 12
num of homozygotes: 205
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-14499477-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499477
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499478
    reference: chr 19
allele count: 6
allele frequency: 4.964257347100873e-5
allele num: 120864
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.168-33dupC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.74-33dupC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.74-33dupC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.74-33dupC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-33dupC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.74-33dupC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.74-33dupC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.74-33dupC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.233-33dupC
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41649
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3084
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

19-14499477-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499477
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499477
    reference: chr 19
allele count: 7095
allele frequency: 5.870234312946783e-2
allele num: 120864
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.168-37A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-37A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.74-37A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.74-37A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.74-37A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.74-37A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.233-37A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.74-37A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.74-37A>G
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 8.75e1
  variant carriers: 276
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 144
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.75e1
  variant carriers: 172
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.75e1
  variant carriers: 171
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 7.75e1
  variant carriers: 218
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 3.25e1
  variant carriers: 197
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 142
genotype depth: GenotypeDepth
  all individuals: 41649
  bin: 9.75e1
  variant carriers: 3802
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.25e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.75e1
  variant carriers: 112
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.25e1
  variant carriers: 167
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 3.75e1
  variant carriers: 179
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 2.25e1
  variant carriers: 178
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 2.75e1
  variant carriers: 226
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 8.25e1
  variant carriers: 236
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.25e1
  variant carriers: 189
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 9.25e1
  variant carriers: 314
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.5e0
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 3.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 3084
  bin: 6.25e1
  variant carriers: 20
num of homozygotes: 199
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/19-14499478-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499478
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499478
    reference: chr 19
allele count: 1
allele frequency: 8.260366760284156e-6
allele num: 121060
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.74-36C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.74-36C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.74-36C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.74-36C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.233-36C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-36C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.74-36C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.168-36C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.74-36C>A
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41641
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3550
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51300
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

19-14499491-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499491
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499491
    reference: chr 19
allele count: 2
allele frequency: 1.651364026686043e-5
allele num: 121112
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.74-23G>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.74-23G>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.168-23G>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.74-23G>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.74-23G>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.74-23G>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.233-23G>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-23G>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.74-23G>T
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41642
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 924
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4133
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

19-14499494-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499494
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499494
    reference: chr 19
allele count: 5
allele frequency: 4.128614602084125e-5
allele num: 121106
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.233-20C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.74-20C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.74-20C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.168-20C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-20C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.74-20C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.74-20C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.74-20C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.74-20C>T
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41643
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51309
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4186
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-14499495-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499495
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499495
    reference: chr 19
allele count: 161
allele frequency: 1.329348041482264e-3
allele num: 121112
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-19G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.168-19G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.74-19G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.74-19G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.74-19G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.74-19G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.74-19G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.233-19G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.74-19G>A
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41675
  bin: 9.75e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 918
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

19-14499495-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499495
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499495
    reference: chr 19
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.74-19G>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.74-19G>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.168-19G>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-19G>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.74-19G>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.74-19G>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.233-19G>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.74-19G>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.74-19G>C
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41675
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1585
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4261
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

19-14499498-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499498
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499498
    reference: chr 19
allele count: 1
allele frequency: 8.254775387561705e-6
allele num: 121142
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.168-16C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.74-16C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.74-16C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.74-16C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-16C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.74-16C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.74-16C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.74-16C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.233-16C>T
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41664
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

19-14499502-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499502
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499502
    reference: chr 19
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.74-12C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.74-12C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-12C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.74-12C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.74-12C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.74-12C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.74-12C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.168-12C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.233-12C>T
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41664
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51310
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

19-14499507-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499507
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499507
    reference: chr 19
allele count: 1
allele frequency: 8.252731654177533e-6
allele num: 121172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.168-7C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-7C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.74-7C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.74-7C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.74-7C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.233-7C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.74-7C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.74-7C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.74-7C>T
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41664
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
hgvs: c.74-7C>T
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

19-14499511-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499511
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499511
    reference: chr 19
allele count: 2
allele frequency: 1.650546330835507e-5
allele num: 121172
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.74-3C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.74-3C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.74-3C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.74-3C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.74-3C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.233-3C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.168-3C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.74-3C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.23-3C>G
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41664
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51312
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
hgvs: c.74-3C>G
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

19-14499522-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499522
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499522
    reference: chr 19
allele count: 2
allele frequency: 1.650410126916539e-5
allele num: 121182
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.82C>T
  hgvsp: ENSP00000242786.4:p.Arg28Trp
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.82C>T
  hgvsp: ENSP00000351413.2:p.Arg28Trp
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.82C>T
  hgvsp: ENSP00000466040.1:p.Arg28Trp
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.241C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.82C>T
  hgvsp: ENSP00000467478.1:p.Arg28Trp
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.31C>T
  hgvsp: ENSP00000467351.1:p.Arg11Trp
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.82C>T
  hgvsp: ENSP00000349918.2:p.Arg28Trp
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.82C>T
  hgvsp: ENSP00000465800.1:p.Arg28Trp
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.176C>T
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41663
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg28Trp
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

19-14499523-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499523
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499523
    reference: chr 19
allele count: 5
allele frequency: 4.125684863687372e-5
allele num: 121192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.32G>A
  hgvsp: ENSP00000467351.1:p.Arg11Gln
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.83G>A
  hgvsp: ENSP00000466040.1:p.Arg28Gln
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.242G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.83G>A
  hgvsp: ENSP00000349918.2:p.Arg28Gln
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.83G>A
  hgvsp: ENSP00000465800.1:p.Arg28Gln
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.83G>A
  hgvsp: ENSP00000242786.4:p.Arg28Gln
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.177G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.83G>A
  hgvsp: ENSP00000351413.2:p.Arg28Gln
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.83G>A
  hgvsp: ENSP00000467478.1:p.Arg28Gln
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41663
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4424
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg28Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

19-14499537-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499537
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499537
    reference: chr 19
allele count: 396
allele frequency: 3.282112486946143e-3
allele num: 120654
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.97A>G
  hgvsp: ENSP00000465800.1:p.Asn33Asp
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.191A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.97A>G
  hgvsp: ENSP00000242786.4:p.Asn33Asp
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.256A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.97A>G
  hgvsp: ENSP00000349918.2:p.Asn33Asp
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.97A>G
  hgvsp: ENSP00000466040.1:p.Asn33Asp
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.46A>G
  hgvsp: ENSP00000467351.1:p.Asn16Asp
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.97A>G
  hgvsp: ENSP00000351413.2:p.Asn33Asp
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.97A>G
  hgvsp: ENSP00000467478.1:p.Asn33Asp
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 8.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 41793
  bin: 9.75e1
  variant carriers: 308
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 8.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 2.5e0
  variant carriers: 3
hgvs: p.Asn33Asp
num of homozygotes: 4
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

19-14499538-ACTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499538
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499535
    reference: chr 19
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.102_104delCTC
  hgvsp: ENSP00000349918.2:p.Ser35del
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.102_104delCTC
  hgvsp: ENSP00000466040.1:p.Ser35del
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.196_198delCTC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.51_53delCTC
  hgvsp: ENSP00000467351.1:p.Ser18del
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.102_104delCTC
  hgvsp: ENSP00000465800.1:p.Ser35del
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.102_104delCTC
  hgvsp: ENSP00000351413.2:p.Ser35del
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.102_104delCTC
  hgvsp: ENSP00000242786.4:p.Ser35del
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.261_263delCTC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.102_104delCTC
  hgvsp: ENSP00000467478.1:p.Ser35del
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41665
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1628
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser35del
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
reference allele: ACTC
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

19-14499539-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499539
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499539
    reference: chr 19
allele count: 2
allele frequency: 1.650110557407346e-5
allele num: 121204
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.99C>T
  hgvsp: ENST00000242786.5:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.99C>T
  hgvsp: ENST00000357355.3:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.99C>T
  hgvsp: ENST00000591080.1:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.99C>T
  hgvsp: ENST00000587606.1:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.99C>T
  hgvsp: ENST00000358600.3:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.48C>T
  hgvsp: ENST00000586517.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.99C>T
  hgvsp: ENST00000592261.2:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.193C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.258C>T
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41664
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 51281
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asn33Asn
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

19-14499544-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499544
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499544
    reference: chr 19
allele count: 10
allele frequency: 8.25000825000825e-5
allele num: 121212
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.263C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.104C>T
  hgvsp: ENSP00000466040.1:p.Ser35Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.198C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.104C>T
  hgvsp: ENSP00000242786.4:p.Ser35Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.104C>T
  hgvsp: ENSP00000467478.1:p.Ser35Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.104C>T
  hgvsp: ENSP00000465800.1:p.Ser35Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.104C>T
  hgvsp: ENSP00000349918.2:p.Ser35Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.53C>T
  hgvsp: ENSP00000467351.1:p.Ser18Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.104C>T
  hgvsp: ENSP00000351413.2:p.Ser35Leu
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41667
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser35Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum

19-14499545-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499545
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499545
    reference: chr 19
allele count: 3
allele frequency: 2.475084152861197e-5
allele num: 121208
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.54G>A
  hgvsp: ENST00000586517.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.105G>A
  hgvsp: ENST00000358600.3:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.105G>A
  hgvsp: ENST00000592261.2:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.199G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.105G>A
  hgvsp: ENST00000587606.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.105G>A
  hgvsp: ENST00000242786.5:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.264G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.105G>A
  hgvsp: ENST00000357355.3:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.105G>A
  hgvsp: ENST00000591080.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41666
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51284
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser35Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

19-14499549-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499549
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499549
    reference: chr 19
allele count: 2
allele frequency: 1.649974425396406e-5
allele num: 121214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.109G>A
  hgvsp: ENSP00000349918.2:p.Val37Ile
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.268G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.109G>A
  hgvsp: ENSP00000466040.1:p.Val37Ile
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.58G>A
  hgvsp: ENSP00000467351.1:p.Val20Ile
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.203G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.109G>A
  hgvsp: ENSP00000467478.1:p.Val37Ile
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.109G>A
  hgvsp: ENSP00000242786.4:p.Val37Ile
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.109G>A
  hgvsp: ENSP00000465800.1:p.Val37Ile
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.109G>A
  hgvsp: ENSP00000351413.2:p.Val37Ile
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41664
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1630
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val37Ile
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

19-14499553-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499553
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499553
    reference: chr 19
allele count: 2
allele frequency: 1.650083329208125e-5
allele num: 121206
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.113A>G
  hgvsp: ENSP00000351413.2:p.Asn38Ser
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.207A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.113A>G
  hgvsp: ENSP00000242786.4:p.Asn38Ser
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.113A>G
  hgvsp: ENSP00000466040.1:p.Asn38Ser
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.113A>G
  hgvsp: ENSP00000467478.1:p.Asn38Ser
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.113A>G
  hgvsp: ENSP00000465800.1:p.Asn38Ser
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.62A>G
  hgvsp: ENSP00000467351.1:p.Asn21Ser
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.113A>G
  hgvsp: ENSP00000349918.2:p.Asn38Ser
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.272A>G
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41663
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4441
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1628
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asn38Ser
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS

19-14499554-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499554
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499554
    reference: chr 19
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.114T>C
  hgvsp: ENST00000591080.1:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.273T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.114T>C
  hgvsp: ENST00000358600.3:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.114T>C
  hgvsp: ENST00000587606.1:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.63T>C
  hgvsp: ENST00000586517.1:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.114T>C
  hgvsp: ENST00000242786.5:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.114T>C
  hgvsp: ENST00000592261.2:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.114T>C
  hgvsp: ENST00000357355.3:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.208T>C
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41663
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51281
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn38Asn
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

19-14499557-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499557
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499557
    reference: chr 19
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.117C>T
  hgvsp: ENST00000592261.2:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.117C>T
  hgvsp: ENST00000591080.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.276C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.117C>T
  hgvsp: ENST00000242786.5:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.117C>T
  hgvsp: ENST00000587606.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.66C>T
  hgvsp: ENST00000586517.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.117C>T
  hgvsp: ENST00000358600.3:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.211C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.117C>T
  hgvsp: ENST00000357355.3:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41664
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala39Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-14499561-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499561
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499561
    reference: chr 19
allele count: 488
allele frequency: 4.026601976995561e-3
allele num: 121194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.121G>A
  hgvsp: ENSP00000466040.1:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.121G>A
  hgvsp: ENSP00000351413.2:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.121G>A
  hgvsp: ENSP00000467478.1:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.280G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.215G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.70G>A
  hgvsp: ENSP00000467351.1:p.Ala24Thr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.121G>A
  hgvsp: ENSP00000242786.4:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.121G>A
  hgvsp: ENSP00000465800.1:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.121G>A
  hgvsp: ENSP00000349918.2:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41729
  bin: 9.75e1
  variant carriers: 459
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4425
  bin: 6.25e1
  variant carriers: 1
hgvs: p.Ala41Thr
num of homozygotes: 12
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

19-14499565-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499565
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499565
    reference: chr 19
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.125G>A
  hgvsp: ENSP00000242786.4:p.Cys42Tyr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.125G>A
  hgvsp: ENSP00000465800.1:p.Cys42Tyr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.125G>A
  hgvsp: ENSP00000349918.2:p.Cys42Tyr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.284G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.74G>A
  hgvsp: ENSP00000467351.1:p.Cys25Tyr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.125G>A
  hgvsp: ENSP00000467478.1:p.Cys42Tyr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.125G>A
  hgvsp: ENSP00000466040.1:p.Cys42Tyr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.219G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.125G>A
  hgvsp: ENSP00000351413.2:p.Cys42Tyr
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41699
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Cys42Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-14499567-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499567
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499567
    reference: chr 19
allele count: 1
allele frequency: 8.251778258214646e-6
allele num: 121186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.221C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.127C>T
  hgvsp: ENSP00000242786.4:p.Arg43Cys
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.286C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.127C>T
  hgvsp: ENSP00000465800.1:p.Arg43Cys
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.127C>T
  hgvsp: ENSP00000466040.1:p.Arg43Cys
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.127C>T
  hgvsp: ENSP00000351413.2:p.Arg43Cys
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.127C>T
  hgvsp: ENSP00000349918.2:p.Arg43Cys
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.76C>T
  hgvsp: ENSP00000467351.1:p.Arg26Cys
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.127C>T
  hgvsp: ENSP00000467478.1:p.Arg43Cys
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41699
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 926
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg43Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

19-14499568-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499568
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499568
    reference: chr 19
allele count: 2
allele frequency: 1.650355651642929e-5
allele num: 121186
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.128G>T
  hgvsp: ENSP00000242786.4:p.Arg43Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.222G>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.128G>T
  hgvsp: ENSP00000465800.1:p.Arg43Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.128G>T
  hgvsp: ENSP00000467478.1:p.Arg43Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.77G>T
  hgvsp: ENSP00000467351.1:p.Arg26Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.128G>T
  hgvsp: ENSP00000349918.2:p.Arg43Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.128G>T
  hgvsp: ENSP00000351413.2:p.Arg43Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.128G>T
  hgvsp: ENSP00000466040.1:p.Arg43Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.287G>T
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41700
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg43Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS

http://identifiers.org/exac.variant/19-14499576-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499576
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499576
    reference: chr 19
allele count: 2
allele frequency: 1.650382888830209e-5
allele num: 121184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.136C>A
  hgvsp: ENSP00000466040.1:p.Pro46Thr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.136C>A
  hgvsp: ENSP00000351413.2:p.Pro46Thr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.230C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.136C>A
  hgvsp: ENSP00000465800.1:p.Pro46Thr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.85C>A
  hgvsp: ENSP00000467351.1:p.Pro29Thr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.136C>A
  hgvsp: ENSP00000242786.4:p.Pro46Thr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.295C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.136C>A
  hgvsp: ENSP00000349918.2:p.Pro46Thr
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.136C>A
  hgvsp: ENSP00000467478.1:p.Pro46Thr
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41699
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro46Thr
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-14499596-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499596
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499596
    reference: chr 19
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.156T>G
  hgvsp: ENST00000242786.5:c.156T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.156T>G
  hgvsp: ENST00000591080.1:c.156T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.156T>G
  hgvsp: ENST00000358600.3:c.156T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.315T>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.156T>G
  hgvsp: ENST00000592261.2:c.156T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.250T>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.105T>G
  hgvsp: ENST00000586517.1:c.105T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.156T>G
  hgvsp: ENST00000357355.3:c.156T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.156T>G
  hgvsp: ENST00000587606.1:c.156T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41700
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51277
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1598
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser52Ser
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

19-14499599-GATC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499599
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499596
    reference: chr 19
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.113_115delTCA
  hgvsp: ENSP00000467351.1:p.Ile38del
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.323_325delTCA
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.164_166delTCA
  hgvsp: ENSP00000242786.4:p.Ile55del
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.164_166delTCA
  hgvsp: ENSP00000465800.1:p.Ile55del
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.164_166delTCA
  hgvsp: ENSP00000466040.1:p.Ile55del
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.164_166delTCA
  hgvsp: ENSP00000351413.2:p.Ile55del
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.258_260delTCA
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.164_166delTCA
  hgvsp: ENSP00000349918.2:p.Ile55del
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.164_166delTCA
  hgvsp: ENSP00000467478.1:p.Ile55del
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41699
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile55del
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: GATC
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

19-14499613-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499613
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499613
    reference: chr 19
allele count: 403
allele frequency: 3.327443565566326e-3
allele num: 121114
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.267C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.122C>T
  hgvsp: ENSP00000467351.1:p.Pro41Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.332C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.173C>T
  hgvsp: ENSP00000466040.1:p.Pro58Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.173C>T
  hgvsp: ENSP00000349918.2:p.Pro58Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.173C>T
  hgvsp: ENSP00000467478.1:p.Pro58Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.173C>T
  hgvsp: ENSP00000465800.1:p.Pro58Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.173C>T
  hgvsp: ENSP00000242786.4:p.Pro58Leu
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.173C>T
  hgvsp: ENSP00000351413.2:p.Pro58Leu
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 41800
  bin: 9.75e1
  variant carriers: 338
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro58Leu
num of homozygotes: 5
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

19-14499614-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499614
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499614
    reference: chr 19
allele count: 2
allele frequency: 1.664364296057121e-5
allele num: 120166
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.174G>A
  hgvsp: ENST00000591080.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.174G>A
  hgvsp: ENST00000592261.2:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.174G>A
  hgvsp: ENST00000587606.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.174G>A
  hgvsp: ENST00000358600.3:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.174G>A
  hgvsp: ENST00000242786.5:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.333G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.268G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.123G>A
  hgvsp: ENST00000586517.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.174G>A
  hgvsp: ENST00000357355.3:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42304
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro58Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

19-14499614-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499614
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499614
    reference: chr 19
allele count: 2938
allele frequency: 2.444951150907911e-2
allele num: 120166
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.174G>C
  hgvsp: ENST00000587606.1:c.174G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.174G>C
  hgvsp: ENST00000591080.1:c.174G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.123G>C
  hgvsp: ENST00000586517.1:c.123G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.174G>C
  hgvsp: ENST00000357355.3:c.174G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.174G>C
  hgvsp: ENST00000242786.5:c.174G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.174G>C
  hgvsp: ENST00000358600.3:c.174G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.174G>C
  hgvsp: ENST00000592261.2:c.174G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.268G>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.333G>C
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 3.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 2.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 8.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 7.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 3.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 8.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 9.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 42304
  bin: 9.75e1
  variant carriers: 2450
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 7.75e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 8.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 6.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 50615
  bin: 9.75e1
  variant carriers: 2569
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 8.75e1
  variant carriers: 25
hgvs: p.Pro58Pro
num of homozygotes: 43
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

19-14499616-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499616
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499616
    reference: chr 19
allele count: 2951
allele frequency: 2.455401717366704e-2
allele num: 120184
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.176C>T
  hgvsp: ENSP00000466040.1:p.Thr59Met
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.335C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.176C>T
  hgvsp: ENSP00000465800.1:p.Thr59Met
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.176C>T
  hgvsp: ENSP00000467478.1:p.Thr59Met
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.125C>T
  hgvsp: ENSP00000467351.1:p.Thr42Met
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.176C>T
  hgvsp: ENSP00000349918.2:p.Thr59Met
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.176C>T
  hgvsp: ENSP00000351413.2:p.Thr59Met
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.176C>T
  hgvsp: ENSP00000242786.4:p.Thr59Met
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.270C>T
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 42313
  bin: 9.75e1
  variant carriers: 2481
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 2.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 8.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 3.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 8.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 4.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 5.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 3.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 7.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 9.25e1
  variant carriers: 45
genotype quality: GenotypeQuality
  all individuals: 50648
  bin: 9.75e1
  variant carriers: 2603
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 8.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.25e1
  variant carriers: 23
hgvs: p.Thr59Met
num of homozygotes: 43
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

19-14499617-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499617
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499617
    reference: chr 19
allele count: 3
allele frequency: 2.477455158061639e-5
allele num: 121092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.177G>A
  hgvsp: ENST00000358600.3:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.126G>A
  hgvsp: ENST00000586517.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.177G>A
  hgvsp: ENST00000587606.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.271G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.177G>A
  hgvsp: ENST00000242786.5:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.336G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.177G>A
  hgvsp: ENST00000591080.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.177G>A
  hgvsp: ENST00000592261.2:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.177G>A
  hgvsp: ENST00000357355.3:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41829
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1584
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr59Thr
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

19-14499629-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499629
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499629
    reference: chr 19
allele count: 5
allele frequency: 4.130183380142078e-5
allele num: 121060
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.189C>T
  hgvsp: ENST00000357355.3:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.189C>T
  hgvsp: ENST00000591080.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.138C>T
  hgvsp: ENST00000586517.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.283C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.189C>T
  hgvsp: ENST00000587606.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.348C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.189C>T
  hgvsp: ENST00000358600.3:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.189C>T
  hgvsp: ENST00000592261.2:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.189C>T
  hgvsp: ENST00000242786.5:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41830
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.75e1
  variant carriers: 0
hgvs: c.189C>T
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

19-14499639-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499639
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499639
    reference: chr 19
allele count: 8
allele frequency: 6.611570247933885e-5
allele num: 121000
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.190+9G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.139+9G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.190+9G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.190+9G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.190+9G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.284+9G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.349+9G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.190+9G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.190+9G>A
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41828
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

19-14499641-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499641
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499641
    reference: chr 19
allele count: 11
allele frequency: 9.095569630719873e-5
allele num: 120938
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.139+11T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.284+11T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.349+11T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.190+11T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.190+11T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.190+11T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.190+11T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.190+11T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.190+11T>C
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41832
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51360
  bin: 9.75e1
  variant carriers: 11
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

19-14499644-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499644
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499644
    reference: chr 19
allele count: 1
allele frequency: 8.267469162340024e-6
allele num: 120956
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.190+14A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.190+14A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.190+14A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.190+14A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.190+14A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.349+14A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.139+14A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.284+14A>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.190+14A>G
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41820
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3937
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ

19-14499646-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499646
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499646
    reference: chr 19
allele count: 1
allele frequency: 8.267195767195768e-6
allele num: 120960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.349+16G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.190+16G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.284+16G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.190+16G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.139+16G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.190+16G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.190+16G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.190+16G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.190+16G>A
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41820
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3991
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-14499647-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499647
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499647
    reference: chr 19
allele count: 5
allele frequency: 4.133666231253823e-5
allele num: 120958
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.139+17G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.190+17G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.349+17G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.190+17G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.190+17G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.190+17G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.284+17G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.190+17G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.190+17G>A
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41820
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum

19-14499651-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499651
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499651
    reference: chr 19
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.190+21C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.190+21C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.190+21C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.190+21C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.190+21C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.349+21C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.284+21C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.190+21C>G
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.139+21C>G
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41820
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

19-14499651-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499651
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499651
    reference: chr 19
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.190+21C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.139+21C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.190+21C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.284+21C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.190+21C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.349+21C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.190+21C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.190+21C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.190+21C>T
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41820
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

19-14499652-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499652
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499652
    reference: chr 19
allele count: 7
allele frequency: 5.788376939106274e-5
allele num: 120932
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.139+22G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.190+22G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.190+22G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.190+22G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.349+22G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.284+22G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.190+22G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.190+22G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.190+22G>A
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41821
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3944
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

19-14499655-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499655
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499655
    reference: chr 19
allele count: 1
allele frequency: 8.269246671628215e-6
allele num: 120930
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.284+25G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.190+25G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.139+25G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.190+25G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.190+25G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.190+25G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.349+25G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.190+25G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.190+25G>A
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41821
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51381
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-14499661-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499661
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499661
    reference: chr 19
allele count: 1
allele frequency: 8.271982794275789e-6
allele num: 120890
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.190+31A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.139+31A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.190+31A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.190+31A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.190+31A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.190+31A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.349+31A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.284+31A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.190+31A>T
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41821
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3450
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

19-14499664-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499664
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499664
    reference: chr 19
allele count: 175
allele frequency: 1.448315815608706e-3
allele num: 120830
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.139+34C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.190+34C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.190+34C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.190+34C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.190+34C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.190+34C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.349+34C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.284+34C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.190+34C>T
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 41832
  bin: 9.75e1
  variant carriers: 145
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3490
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1406
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 7.25e1
  variant carriers: 4
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

19-14499665-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499665
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499665
    reference: chr 19
allele count: 5
allele frequency: 4.136949578858533e-5
allele num: 120862
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.190+35G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.190+35G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.284+35G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.190+35G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.190+35G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.139+35G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.349+35G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.190+35G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.190+35G>A
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41830
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3350
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

19-14499666-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499666
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499666
    reference: chr 19
allele count: 72
allele frequency: 5.957010242748168e-4
allele num: 120866
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.190+36C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.190+36C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.139+36C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.349+36C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.284+36C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.190+36C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.190+36C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.190+36C>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.190+36C>T
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 41836
  bin: 9.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 881
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3374
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

19-14499667-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499667
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499667
    reference: chr 19
allele count: 1
allele frequency: 8.273214640280627e-6
allele num: 120872
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.190+37G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.190+37G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.190+37G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.349+37G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.190+37G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.190+37G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.190+37G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.139+37G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.284+37G>A
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41833
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3340
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1381
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum

19-14499670-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499670
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499671
    reference: chr 19
allele count: 1
allele frequency: 8.27348843366317e-6
allele num: 120868
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.190+40_190+41insG
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.139+40_139+41insG
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.190+40_190+41insG
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.284+40_284+41insG
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.190+40_190+41insG
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.349+40_349+41insG
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.190+40_190+41insG
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.190+40_190+41insG
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.190+40_190+41insG
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41833
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

19-14499680-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14499680
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14499680
    reference: chr 19
allele count: 210
allele frequency: 1.738842427755237e-3
allele num: 120770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.190+50T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.190+50T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.190+50T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.349+50T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.139+50T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.190+50T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.284+50T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.190+50T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.190+50T>A
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 41836
  bin: 9.75e1
  variant carriers: 171
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

19-14501692-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14501692
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14501692
    reference: chr 19
allele count: 6
allele frequency: 5.617977528089888e-5
allele num: 106800
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.350-44A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.191-44A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.191-44A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.191-44A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.191-44A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.140-44A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.285-44A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.191-44A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.191-44A>T
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16993
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6793
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12115
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1779
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4067
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 7370
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-14501697-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14501697
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14501697
    reference: chr 19
allele count: 1
allele frequency: 9.360666479453337e-6
allele num: 106830
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.191-39C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.285-39C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.191-39C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.191-39C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.191-39C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.350-39C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.191-39C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.140-39C>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.191-39C>A
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6755
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9594
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3380
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2414
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4007
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-14501699-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14501699
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14501699
    reference: chr 19
allele count: 1
allele frequency: 9.334279206959638e-6
allele num: 107132
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.191-37T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.191-37T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.140-37T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.191-37T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.285-37T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.191-37T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.350-37T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.191-37T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.191-37T>C
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8580
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16041
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6753
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6535
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22915
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3962
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2446
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum

19-14501709-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14501709
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14501709
    reference: chr 19
allele count: 1
allele frequency: 9.251378455389853e-6
allele num: 108092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.191-27G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.191-27G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.140-27G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.285-27G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.191-27G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.350-27G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.191-27G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.191-27G>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.191-27G>A
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8859
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5761
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1814
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3596
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7258
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

19-14501711-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14501711
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14501711
    reference: chr 19
allele count: 16
allele frequency: 1.47413808988557e-4
allele num: 108538
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.140-25G>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.191-25G>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.191-25G>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.191-25G>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.191-25G>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.350-25G>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.285-25G>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.191-25G>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.191-25G>C
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9314
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12234
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24885
  bin: 2.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 7119
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4348
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1532
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP

19-14501712-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14501712
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14501712
    reference: chr 19
allele count: 178
allele frequency: 1.634407022440959e-3
allele num: 108908
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.350-24A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.191-24A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.191-24A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.191-24A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.140-24A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.191-24A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.191-24A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.285-24A>T
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.191-24A>T
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11797
  bin: 1.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6025
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9416
  bin: 2.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 4822
  bin: 1.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 3.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25599
  bin: 2.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3296
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5375
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31123
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-14501714-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14501714
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14501714
    reference: chr 19
allele count: 1
allele frequency: 9.143275121148396e-6
allele num: 109370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.140-22T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.191-22T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.191-22T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.350-22T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.285-22T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.191-22T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.191-22T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.191-22T>A
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.191-22T>A
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9684
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6784
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4908
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33654
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS

19-14501714-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14501714
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14501714
    reference: chr 19
allele count: 1
allele frequency: 9.143275121148396e-6
allele num: 109370
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.191-22T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.191-22T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.350-22T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.191-22T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.191-22T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.140-22T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.191-22T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.191-22T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.285-22T>C
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10723
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33654
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

19-14501714-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14501714
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14501713
    reference: chr 19
allele count: 2
allele frequency: 1.828655024229679e-5
allele num: 109370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.285-19delC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.191-19delC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.191-19delC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.191-19delC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.350-19delC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.191-19delC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.191-19delC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.140-19delC
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.191-19delC
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10723
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6784
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1187
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: TC
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

19-14501720-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14501720
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 14501720
    reference: chr 19
allele count: 1
allele frequency: 9.00284489898808e-6
allele num: 111076
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467351
  ensembl transcript: ENST00000586517
  gene symbol: CD97
  hgvsc: ENST00000586517.1:c.140-16T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000349918
  ensembl transcript: ENST00000357355
  gene symbol: CD97
  hgvsc: ENST00000357355.3:c.191-16T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000465800
  ensembl transcript: ENST00000587606
  gene symbol: CD97
  hgvsc: ENST00000587606.1:c.191-16T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000466040
  ensembl transcript: ENST00000591080
  gene symbol: CD97
  hgvsc: ENST00000591080.1:c.191-16T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000242786
  ensembl transcript: ENST00000242786
  gene symbol: CD97
  hgvsc: ENST00000242786.5:c.191-16T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587535
  gene symbol: CD97
  hgvsc: ENST00000587535.1:n.350-16T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000351413
  ensembl transcript: ENST00000358600
  gene symbol: CD97
  hgvsc: ENST00000358600.3:c.191-16T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl transcript: ENST00000587728
  gene symbol: CD97
  hgvsc: ENST00000587728.1:n.285-16T>C
  variant of: http://identifiers.org/hgnc/1711
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123146
  ensembl protein: ENSP00000467478
  ensembl transcript: ENST00000592261
  gene symbol: CD97
  hgvsc: ENST00000592261.2:c.191-16T>C
  variant of: http://identifiers.org/hgnc/1711
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8090
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 279
bin: 7.75e1
variant carriers: 12

GenotypeQuality
all individuals: 614
bin: 4.75e1
variant carriers: 14

GenotypeQuality
all individuals: 1868
bin: 3.75e1
variant carriers: 8

GenotypeQuality
all individuals: 151
bin: 8.25e1
variant carriers: 6

GenotypeQuality
all individuals: 5350
bin: 7.5e0
variant carriers: 7

GenotypeQuality
all individuals: 554
bin: 4.25e1
variant carriers: 9

GenotypeQuality
all individuals: 9751
bin: 6.25e1
variant carriers: 10

GenotypeQuality
all individuals: 1289
bin: 1.25e1
variant carriers: 7

GenotypeQuality
all individuals: 384
bin: 5.25e1
variant carriers: 10

GenotypeQuality
all individuals: 1899
bin: 9.75e1
variant carriers: 307

GenotypeQuality
all individuals: 252
bin: 7.25e1
variant carriers: 12

GenotypeQuality
all individuals: 1214
bin: 6.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1163
bin: 1.75e1
variant carriers: 11

GenotypeQuality
all individuals: 73
bin: 8.75e1
variant carriers: 14

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

Latino
type: Population
allele count: 12
allele frequency: 2.822201317027281e-3
allele num: 4252
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 2.949219797308167e-4
allele num: 37298
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.286008230452675e-4
allele num: 7776
num of homozygotes: 0

African
type: Population
allele count: 344
allele frequency: 7.214765100671142e-2
allele num: 4768
num of homozygotes: 4

Other
type: Population
allele count: 2
allele frequency: 4.132231404958678e-3
allele num: 484
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.46199e5

FS
type: SiteQuality
SIO_000300: 3.341e0

MQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.965e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.133e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.054e1

MQ
type: SiteQuality
SIO_000300: 3.185e1

GenotypeQuality
all individuals: 1310
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1647
bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
all individuals: 580
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1460
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26382
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 167
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3342
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12268
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3754
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4940
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.577186742951394e-5
allele num: 38802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8062
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4766
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.938e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.03e-2

FS
type: SiteQuality
SIO_000300: 1.451e0

DP
type: SiteQuality
SIO_000300: 8.89901e5

MQ
type: SiteQuality
SIO_000300: 3.263e1

MQRankSum
type: SiteQuality
SIO_000300: 6.04e-1

GenotypeQuality
all individuals: 3152
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
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variant carriers: 0

GenotypeQuality
all individuals: 13495
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GenotypeQuality
all individuals: 1651
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variant carriers: 1

GenotypeQuality
all individuals: 264
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GenotypeQuality
all individuals: 26222
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GenotypeQuality
all individuals: 561
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GenotypeQuality
all individuals: 1098
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3183
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variant carriers: 0

GenotypeQuality
all individuals: 307
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variant carriers: 0

GenotypeQuality
all individuals: 101
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variant carriers: 0

GenotypeQuality
all individuals: 1567
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5032
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.531901964755925e-5
allele num: 39496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4696
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.6e0

FS
type: SiteQuality
SIO_000300: 1.657e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.599999999999999e-3

QD
type: SiteQuality
SIO_000300: 6.94e0

DP
type: SiteQuality
SIO_000300: 9.05041e5

MQ
type: SiteQuality
SIO_000300: 3.421e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.292e0

GenotypeQuality
all individuals: 4504
bin: 3.25e1
variant carriers: 4502

GenotypeQuality
all individuals: 2517
bin: 6.75e1
variant carriers: 2516

GenotypeQuality
all individuals: 4606
bin: 3.75e1
variant carriers: 4605

GenotypeQuality
all individuals: 4450
bin: 2.25e1
variant carriers: 4432

GenotypeQuality
all individuals: 865
bin: 9.25e1
variant carriers: 865

GenotypeQuality
all individuals: 3237
bin: 2.75e1
variant carriers: 3230

GenotypeQuality
all individuals: 1985
bin: 5.75e1
variant carriers: 1985

GenotypeQuality
all individuals: 6298
bin: 9.75e1
variant carriers: 6298

GenotypeQuality
all individuals: 3690
bin: 5.25e1
variant carriers: 3690

GenotypeQuality
all individuals: 745
bin: 8.75e1
variant carriers: 745

GenotypeQuality
all individuals: 2681
bin: 2.5e0
variant carriers: 2511

GenotypeQuality
all individuals: 2797
bin: 4.25e1
variant carriers: 2797

GenotypeQuality
all individuals: 2955
bin: 6.25e1
variant carriers: 2949

GenotypeQuality
all individuals: 3844
bin: 1.75e1
variant carriers: 3844

European (Finnish)
type: Population
allele count: 4485
allele frequency: 8.89527965093217e-1
allele num: 5042
num of homozygotes: 1964

Other
type: Population
allele count: 537
allele frequency: 8.689320388349514e-1
allele num: 618
num of homozygotes: 228

Latino
type: Population
allele count: 7383
allele frequency: 9.155505952380952e-1
allele num: 8064
num of homozygotes: 3352

African
type: Population
allele count: 5549
allele frequency: 8.208579881656805e-1
allele num: 6760
num of homozygotes: 2187

South Asian
type: Population
allele count: 10017
allele frequency: 9.099745639534884e-1
allele num: 11008
num of homozygotes: 4513

East Asian
type: Population
allele count: 5720
allele frequency: 9.067850348763475e-1
allele num: 6308
num of homozygotes: 2567

European (Non-Finnish)
type: Population
allele count: 41007
allele frequency: 8.761056274836559e-1
allele num: 46806
num of homozygotes: 17606

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 3.67e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.07e-1

QD
type: SiteQuality
SIO_000300: 2.969e1

FS
type: SiteQuality
SIO_000300: 5.401e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.357e-1

DP
type: SiteQuality
SIO_000300: 1.241803e6

GenotypeQuality
all individuals: 1204
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4019
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3797
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2864
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1712
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4950
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1593
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variant carriers: 0

GenotypeQuality
all individuals: 5266
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 768
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variant carriers: 0

GenotypeQuality
all individuals: 7676
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4913
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2707
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7676
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7656
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9972
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.79058896852602e-5
allele num: 12836
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

FS
type: SiteQuality
SIO_000300: 1.0372e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e0

VQSLOD
type: SiteQuality
SIO_000300: -2.915e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

DP
type: SiteQuality
SIO_000300: 1.266274e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 4.325e1

GenotypeQuality
all individuals: 159
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1373
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 379
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variant carriers: 0

GenotypeQuality
all individuals: 2558
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 924
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variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

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

GenotypeQuality
all individuals: 51587
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 516
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variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
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: 1.503849855630414e-5
allele num: 66496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.985e1

MQ
type: SiteQuality
SIO_000300: 4.479e1

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

MQRankSum
type: SiteQuality
SIO_000300: -5.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.126e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.753e0

DP
type: SiteQuality
SIO_000300: 6.589948e6

GenotypeQuality
all individuals: 164
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1364
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51588
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2810
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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: 11572
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: 10322
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.246542101431691e-4
allele num: 16484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66492
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.448e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.253e0

DP
type: SiteQuality
SIO_000300: 6.590153e6

MQRankSum
type: SiteQuality
SIO_000300: 5.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.416e0

QD
type: SiteQuality
SIO_000300: 1.224e1

FS
type: SiteQuality
SIO_000300: 6.432e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.82e-1

GenotypeQuality
all individuals: 571
bin: 7.25e1
variant carriers: 15

GenotypeQuality
all individuals: 2663
bin: 6.25e1
variant carriers: 23

GenotypeQuality
all individuals: 132
bin: 2.5e0
variant carriers: 11

GenotypeQuality
all individuals: 210
bin: 3.25e1
variant carriers: 14

GenotypeQuality
all individuals: 163
bin: 2.75e1
variant carriers: 13

GenotypeQuality
all individuals: 238
bin: 3.75e1
variant carriers: 14

GenotypeQuality
all individuals: 55
bin: 1.75e1
variant carriers: 10

GenotypeQuality
all individuals: 230
bin: 5.25e1
variant carriers: 21

GenotypeQuality
all individuals: 269
bin: 4.75e1
variant carriers: 12

GenotypeQuality
all individuals: 761
bin: 7.75e1
variant carriers: 14

GenotypeQuality
all individuals: 529
bin: 8.25e1
variant carriers: 20

GenotypeQuality
all individuals: 290
bin: 8.75e1
variant carriers: 25

GenotypeQuality
all individuals: 184
bin: 4.25e1
variant carriers: 18

GenotypeQuality
all individuals: 423
bin: 9.25e1
variant carriers: 25

South Asian
type: Population
allele count: 538
allele frequency: 3.307512602975532e-2
allele num: 16266
num of homozygotes: 7

East Asian
type: Population
allele count: 164
allele frequency: 1.897708863688961e-2
allele num: 8642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1448
allele frequency: 2.17940999397953e-2
allele num: 66440
num of homozygotes: 1

Other
type: Population
allele count: 44
allele frequency: 4.899777282850779e-2
allele num: 898
num of homozygotes: 0

Latino
type: Population
allele count: 1635
allele frequency: 1.414604602872469e-1
allele num: 11558
num of homozygotes: 18

European (Finnish)
type: Population
allele count: 155
allele frequency: 2.34351375869368e-2
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 3236
allele frequency: 3.170683911424652e-1
allele num: 10206
num of homozygotes: 179

VQSLOD
type: SiteQuality
SIO_000300: -8.794e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.73e-1

MQ
type: SiteQuality
SIO_000300: 4.289e1

DP
type: SiteQuality
SIO_000300: 6.609358e6

FS
type: SiteQuality
SIO_000300: 2.579e0

QD
type: SiteQuality
SIO_000300: 1.247e1

MQRankSum
type: SiteQuality
SIO_000300: 5.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e0

GenotypeQuality
all individuals: 427
bin: 9.25e1
variant carriers: 27

GenotypeQuality
all individuals: 102
bin: 5.75e1
variant carriers: 14

GenotypeQuality
all individuals: 767
bin: 7.75e1
variant carriers: 14

GenotypeQuality
all individuals: 148
bin: 5.25e1
variant carriers: 24

GenotypeQuality
all individuals: 169
bin: 4.25e1
variant carriers: 16

GenotypeQuality
all individuals: 102
bin: 2.5e0
variant carriers: 12

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 11

GenotypeQuality
all individuals: 52324
bin: 9.75e1
variant carriers: 6791

GenotypeQuality
all individuals: 579
bin: 7.25e1
variant carriers: 16

GenotypeQuality
all individuals: 162
bin: 2.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1248
bin: 6.75e1
variant carriers: 20

GenotypeQuality
all individuals: 2809
bin: 6.25e1
variant carriers: 23

GenotypeQuality
all individuals: 531
bin: 8.25e1
variant carriers: 19

GenotypeQuality
all individuals: 293
bin: 8.75e1
variant carriers: 21

Latino
type: Population
allele count: 1638
allele frequency: 1.41597510373444e-1
allele num: 11568
num of homozygotes: 19

South Asian
type: Population
allele count: 537
allele frequency: 3.2856093979442e-2
allele num: 16344
num of homozygotes: 7

African
type: Population
allele count: 3240
allele frequency: 3.169014084507042e-1
allele num: 10224
num of homozygotes: 178

Other
type: Population
allele count: 44
allele frequency: 4.899777282850779e-2
allele num: 898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 155
allele frequency: 2.34351375869368e-2
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1450
allele frequency: 2.18209179834462e-2
allele num: 66450
num of homozygotes: 1

East Asian
type: Population
allele count: 164
allele frequency: 1.897708863688961e-2
allele num: 8642
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.184e1

VQSLOD
type: SiteQuality
SIO_000300: -1.042e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.2e-2

MQ
type: SiteQuality
SIO_000300: 4.317e1

DP
type: SiteQuality
SIO_000300: 6.640407e6

MQRankSum
type: SiteQuality
SIO_000300: 4.98e-1

FS
type: SiteQuality
SIO_000300: 3.618e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e0

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1284
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52312
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 586
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66434
num of homozygotes: 0

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

East Asian
type: Population
allele count: 6
allele frequency: 6.941230911614993e-4
allele num: 8644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.057e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.2e-1

DP
type: SiteQuality
SIO_000300: 6.697389e6

MQ
type: SiteQuality
SIO_000300: 4.376e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

FS
type: SiteQuality
SIO_000300: 4.579e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-1

GenotypeQuality
all individuals: 426
bin: 9.25e1
variant carriers: 21

GenotypeQuality
all individuals: 216
bin: 2.25e1
variant carriers: 12

GenotypeQuality
all individuals: 542
bin: 8.25e1
variant carriers: 21

GenotypeQuality
all individuals: 144
bin: 4.25e1
variant carriers: 18

GenotypeQuality
all individuals: 52312
bin: 9.75e1
variant carriers: 6671

GenotypeQuality
all individuals: 144
bin: 2.75e1
variant carriers: 13

GenotypeQuality
all individuals: 184
bin: 3.25e1
variant carriers: 10

GenotypeQuality
all individuals: 159
bin: 4.75e1
variant carriers: 13

GenotypeQuality
all individuals: 778
bin: 7.75e1
variant carriers: 16

GenotypeQuality
all individuals: 586
bin: 7.25e1
variant carriers: 17

GenotypeQuality
all individuals: 297
bin: 8.75e1
variant carriers: 25

GenotypeQuality
all individuals: 1284
bin: 6.75e1
variant carriers: 15

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 9

GenotypeQuality
all individuals: 105
bin: 5.25e1
variant carriers: 17

Latino
type: Population
allele count: 1634
allele frequency: 1.413494809688581e-1
allele num: 11560
num of homozygotes: 17

East Asian
type: Population
allele count: 164
allele frequency: 1.897269782508098e-2
allele num: 8644
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 155
allele frequency: 2.34351375869368e-2
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 3213
allele frequency: 3.125486381322957e-1
allele num: 10280
num of homozygotes: 175

South Asian
type: Population
allele count: 525
allele frequency: 3.194985394352483e-2
allele num: 16432
num of homozygotes: 6

European (Non-Finnish)
type: Population
allele count: 1360
allele frequency: 2.047144534425144e-2
allele num: 66434
num of homozygotes: 1

Other
type: Population
allele count: 44
allele frequency: 4.888888888888889e-2
allele num: 900
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.057e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
SIO_000300: 4.579e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-1

DP
type: SiteQuality
SIO_000300: 6.697389e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

MQ
type: SiteQuality
SIO_000300: 4.376e1

GenotypeQuality
all individuals: 123
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1481
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 917
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 491
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 668
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503895088278642e-5
allele num: 66494
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.5e0

VQSLOD
type: SiteQuality
SIO_000300: -2.145e0

QD
type: SiteQuality
SIO_000300: 7.31e0

MQ
type: SiteQuality
SIO_000300: 4.371e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.09e-1

DP
type: SiteQuality
SIO_000300: 6.685288e6

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

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51306
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 89
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 122
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1550
bin: 6.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
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: 2
allele frequency: 1.932367149758454e-4
allele num: 10350
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.567e0

MQRankSum
type: SiteQuality
SIO_000300: 2.94e-1

DP
type: SiteQuality
SIO_000300: 6.688714e6

FS
type: SiteQuality
SIO_000300: 1.872e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.500999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

MQ
type: SiteQuality
SIO_000300: 4.48e1

QD
type: SiteQuality
SIO_000300: 2.731e1

GenotypeQuality
all individuals: 922
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 209
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503623733197005e-5
allele num: 66506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.423948612289419e-4
allele num: 16502
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.685e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

QD
type: SiteQuality
SIO_000300: 1.331e1

DP
type: SiteQuality
SIO_000300: 6.689856e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.668e0

MQRankSum
type: SiteQuality
SIO_000300: 9.16e-1

FS
type: SiteQuality
SIO_000300: 1.964e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

GenotypeQuality
all individuals: 68
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 196
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1585
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51306
bin: 9.75e1
variant carriers: 154

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 4261
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 492
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.516084420660213e-5
allele num: 66524
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: 4
allele frequency: 3.455425017277125e-4
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 150
allele frequency: 1.450676982591876e-2
allele num: 10340
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 2.759e0

QD
type: SiteQuality
SIO_000300: 9.18e0

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.214e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQ
type: SiteQuality
SIO_000300: 4.457e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e-1

DP
type: SiteQuality
SIO_000300: 6.694954e6

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 68
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 51306
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503216884132043e-5
allele num: 66524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
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: -1.214e0

MQ
type: SiteQuality
SIO_000300: 4.457e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e-1

FS
type: SiteQuality
SIO_000300: 2.759e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-1

DP
type: SiteQuality
SIO_000300: 6.694954e6

QD
type: SiteQuality
SIO_000300: 9.18e0

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

GenotypeQuality
all individuals: 51311
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1596
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 924
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4304
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
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: 66536
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: 906
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: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 4.481e1

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-1

DP
type: SiteQuality
SIO_000300: 6.693547e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e0

VQSLOD
type: SiteQuality
SIO_000300: -3.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.513e0

QD
type: SiteQuality
SIO_000300: 1.002e1

FS
type: SiteQuality
SIO_000300: 5.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.936e0

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

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

GenotypeQuality
all individuals: 53
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 927
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4379
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1596
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 66546
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.477e0

DP
type: SiteQuality
SIO_000300: 6.694063e6

FS
type: SiteQuality
SIO_000300: 2.003e0

QD
type: SiteQuality
SIO_000300: 1.293e1

MQ
type: SiteQuality
SIO_000300: 4.443e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.45e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.007e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

GenotypeQuality
all individuals: 150
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 332
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 928
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1606
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51310
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 493
bin: 9.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
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: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66556
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e0

FS
type: SiteQuality
SIO_000300: 7.126e0

VQSLOD
type: SiteQuality
SIO_000300: -2.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.062e0

MQ
type: SiteQuality
SIO_000300: 4.492e1

MQRankSum
type: SiteQuality
SIO_000300: 8.81e-1

QD
type: SiteQuality
SIO_000300: 1.04e1

DP
type: SiteQuality
SIO_000300: 6.694517e6

GenotypeQuality
all individuals: 1614
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 688
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4401
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 928
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
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: 66550
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.935e0

QD
type: SiteQuality
SIO_000300: 1.551e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.188e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 8.169e0

DP
type: SiteQuality
SIO_000300: 6.694781e6

MQ
type: SiteQuality
SIO_000300: 4.551e1

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 688
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 493
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51313
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4413
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1623
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004988280545706e-5
allele num: 66556
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.752e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.144e0

MQRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.05e0

VQSLOD
type: SiteQuality
SIO_000300: -9.836e-1

MQ
type: SiteQuality
SIO_000300: 4.727e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.71e-1

DP
type: SiteQuality
SIO_000300: 6.695329e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 2.986e1

GenotypeQuality
all individuals: 137
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 929
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1626
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51313
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004536850644473e-5
allele num: 66566
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
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: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
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: 1.276e1

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.51e-1

DP
type: SiteQuality
SIO_000300: 6.69553e6

FS
type: SiteQuality
SIO_000300: 3.216e0

MQ
type: SiteQuality
SIO_000300: 4.729e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.576e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.1e-1

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 5

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 6

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 148
bin: 2.25e1
variant carriers: 6

GenotypeQuality
all individuals: 1605
bin: 6.75e1
variant carriers: 7

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 327
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 488
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 676
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 4397
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 57
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 611
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 50951
bin: 9.75e1
variant carriers: 339

African
type: Population
allele count: 27
allele frequency: 2.618816682832202e-3
allele num: 10310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 26
allele frequency: 3.963414634146342e-3
allele num: 6560
num of homozygotes: 0

East Asian
type: Population
allele count: 11
allele frequency: 1.27373784159333e-3
allele num: 8636
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 6.666666666666667e-3
allele num: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 262
allele frequency: 1.589227223098387e-2
allele num: 16486
num of homozygotes: 4

European (Non-Finnish)
type: Population
allele count: 56
allele frequency: 8.452830188679245e-4
allele num: 66250
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 6.949270326615705e-4
allele num: 11512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.181e0

FS
type: SiteQuality
SIO_000300: 3.991e0

MQ
type: SiteQuality
SIO_000300: 4.826e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.284e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.63e-1

QD
type: SiteQuality
SIO_000300: 4.57e0

DP
type: SiteQuality
SIO_000300: 6.736863e6

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

GenotypeQuality
all individuals: 4464
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 494
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 330
bin: 8.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 620
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 929
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51287
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 682
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50195253829979e-5
allele num: 66580
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.773e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.22e-1

MQ
type: SiteQuality
SIO_000300: 4.851e1

VQSLOD
type: SiteQuality
SIO_000300: 3.91e0

DP
type: SiteQuality
SIO_000300: 6.691423e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.79e-1

QD
type: SiteQuality
SIO_000300: 1.664e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e-2

GenotypeQuality
all individuals: 619
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4477
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1629
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 682
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 330
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66580
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.734e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 4.827e1

VQSLOD
type: SiteQuality
SIO_000300: -3.432e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.49e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.392e0

QD
type: SiteQuality
SIO_000300: 1.36e0

DP
type: SiteQuality
SIO_000300: 6.691245e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

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

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

GenotypeQuality
all individuals: 4474
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51283
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 133
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 928
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 619
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1630
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003544182134919e-5
allele num: 66588
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.821600771456124e-4
allele num: 10370
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: 904
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.592016588906169e-4
allele num: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.05e-1

MQ
type: SiteQuality
SIO_000300: 5.124e1

BaseQRankSum
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QD
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ReadPosRankSum
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FS
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VQSLOD
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DP
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InbreedingCoeff
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SIO_000300: -2.0e-4

MQRankSum
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GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.501862309263487e-5
allele num: 66584
num of homozygotes: 0

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

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

Latino
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allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

East Asian
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ClippingRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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DP
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FS
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QD
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 904
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
allele num: 11574
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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: 9.643201542912247e-5
allele num: 10370
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.501726986033939e-5
allele num: 66590
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MQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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FS
type: SiteQuality
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MQ
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ClippingRankSum
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InbreedingCoeff
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QD
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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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Other
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allele frequency: 0.0e0
allele num: 904
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10370
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
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Latino
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
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European (Non-Finnish)
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allele frequency: 1.501907422426482e-5
allele num: 66582
num of homozygotes: 0

QD
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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DP
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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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

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

African
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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DP
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FS
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QD
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ReadPosRankSum
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 5.142e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 11574
num of homozygotes: 0

South Asian
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allele num: 16512
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East Asian
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
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African
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European (Finnish)
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FS
type: SiteQuality
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QD
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MQRankSum
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DP
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VQSLOD
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BaseQRankSum
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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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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European (Non-Finnish)
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allele num: 66574
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East Asian
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European (Finnish)
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African
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Latino
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Other
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South Asian
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VQSLOD
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InbreedingCoeff
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QD
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ClippingRankSum
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DP
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BaseQRankSum
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FS
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MQRankSum
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MQ
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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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European (Non-Finnish)
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South Asian
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African
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European (Finnish)
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Latino
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East Asian
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Other
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MQRankSum
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MQ
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BaseQRankSum
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VQSLOD
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DP
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QD
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ReadPosRankSum
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FS
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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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European (Non-Finnish)
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East Asian
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Other
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African
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European (Finnish)
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Latino
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South Asian
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VQSLOD
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DP
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ReadPosRankSum
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FS
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MQ
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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QD
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SIO_000300: 1.37e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.425e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -5.521e-1

QD
type: SiteQuality
SIO_000300: 1.283e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.28e-1

DP
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MQ
type: SiteQuality
SIO_000300: 5.415e1

MQRankSum
type: SiteQuality
SIO_000300: 7.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

FS
type: SiteQuality
SIO_000300: 1.746e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004536850644473e-5
allele num: 66566
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-2

MQRankSum
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SIO_000300: 1.95e0

InbreedingCoeff
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SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 6.696887e6

FS
type: SiteQuality
SIO_000300: 1.177e0

QD
type: SiteQuality
SIO_000300: 1.258e1

VQSLOD
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SIO_000300: -1.556e0

MQ
type: SiteQuality
SIO_000300: 5.524e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.674e0

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
all individuals: 926
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
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: 11570
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.9801e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

QD
type: SiteQuality
SIO_000300: 1.178e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.53e-1

MQ
type: SiteQuality
SIO_000300: 5.45e1

DP
type: SiteQuality
SIO_000300: 6.695715e6

GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502810255177181e-5
allele num: 66542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 3.171e0

MQRankSum
type: SiteQuality
SIO_000300: -1.007e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 5.585e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.38e-1

QD
type: SiteQuality
SIO_000300: 1.685e1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 6.695394e6

GenotypeQuality
all individuals: 913
bin: 7.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 396

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 2
allele frequency: 2.2271714922049e-3
allele num: 898
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 16
allele frequency: 1.38264777048047e-3
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.05234673321507e-4
allele num: 66518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 378
allele frequency: 3.64724044770359e-2
allele num: 10364
num of homozygotes: 5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 1.095e0

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

DP
type: SiteQuality
SIO_000300: 6.727644e6

QD
type: SiteQuality
SIO_000300: 1.385e1

MQRankSum
type: SiteQuality
SIO_000300: 8.55e-1

MQ
type: SiteQuality
SIO_000300: 5.751e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.26e-2

GenotypeQuality
all individuals: 64
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 915
bin: 7.75e1
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GenotypeQuality
all individuals: 98
bin: 2.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.021239312365933e-5
allele num: 66198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11212
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e0

VQSLOD
type: SiteQuality
SIO_000300: -6.462e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e0

MQ
type: SiteQuality
SIO_000300: 5.564e1

FS
type: SiteQuality
SIO_000300: 1.074e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.579e0

MQRankSum
type: SiteQuality
SIO_000300: -5.037e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.05e-2

QD
type: SiteQuality
SIO_000300: 2.94e0

DP
type: SiteQuality
SIO_000300: 6.810098e6

GenotypeQuality
all individuals: 672
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variant carriers: 14

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 16

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 64
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GenotypeQuality
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GenotypeQuality
all individuals: 506
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GenotypeQuality
all individuals: 73
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variant carriers: 24

GenotypeQuality
all individuals: 98
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GenotypeQuality
all individuals: 915
bin: 7.75e1
variant carriers: 26

East Asian
type: Population
allele count: 142
allele frequency: 1.652315569001629e-2
allele num: 8594
num of homozygotes: 0

Latino
type: Population
allele count: 1119
allele frequency: 9.980378166250446e-2
allele num: 11212
num of homozygotes: 21

European (Non-Finnish)
type: Population
allele count: 1055
allele frequency: 1.59370373727303e-2
allele num: 66198
num of homozygotes: 5

European (Finnish)
type: Population
allele count: 111
allele frequency: 1.685905224787363e-2
allele num: 6584
num of homozygotes: 1

African
type: Population
allele count: 212
allele frequency: 2.055458599961218e-2
allele num: 10314
num of homozygotes: 5

Other
type: Population
allele count: 20
allele frequency: 2.242152466367713e-2
allele num: 892
num of homozygotes: 1

South Asian
type: Population
allele count: 279
allele frequency: 1.704129000732959e-2
allele num: 16372
num of homozygotes: 10

DP
type: SiteQuality
SIO_000300: 6.810098e6

MQRankSum
type: SiteQuality
SIO_000300: -5.037e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.05e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.579e0

FS
type: SiteQuality
SIO_000300: 1.074e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e0

QD
type: SiteQuality
SIO_000300: 2.94e0

MQ
type: SiteQuality
SIO_000300: 5.564e1

VQSLOD
type: SiteQuality
SIO_000300: -6.462e0

GenotypeQuality
all individuals: 57
bin: 7.5e0
variant carriers: 16

GenotypeQuality
all individuals: 245
bin: 2.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 1568
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variant carriers: 28

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 100
bin: 2.75e1
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GenotypeQuality
all individuals: 914
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variant carriers: 24

GenotypeQuality
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GenotypeQuality
all individuals: 500
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GenotypeQuality
all individuals: 678
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GenotypeQuality
all individuals: 62
bin: 1.25e1
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GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 22

GenotypeQuality
all individuals: 67
bin: 3.75e1
variant carriers: 24

GenotypeQuality
all individuals: 607
bin: 8.25e1
variant carriers: 20

Other
type: Population
allele count: 20
allele frequency: 2.242152466367713e-2
allele num: 892
num of homozygotes: 1

Latino
type: Population
allele count: 1116
allele frequency: 9.969626585670895e-2
allele num: 11194
num of homozygotes: 21

European (Finnish)
type: Population
allele count: 111
allele frequency: 1.685905224787363e-2
allele num: 6584
num of homozygotes: 1

African
type: Population
allele count: 214
allele frequency: 2.074045357627447e-2
allele num: 10318
num of homozygotes: 5

South Asian
type: Population
allele count: 279
allele frequency: 1.703920850128252e-2
allele num: 16374
num of homozygotes: 10

East Asian
type: Population
allele count: 147
allele frequency: 1.710495694670701e-2
allele num: 8594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1064
allele frequency: 1.606571238750982e-2
allele num: 66228
num of homozygotes: 5

FS
type: SiteQuality
SIO_000300: 8.265000000000001e0

DP
type: SiteQuality
SIO_000300: 6.816189e6

MQ
type: SiteQuality
SIO_000300: 5.579e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.245e0

MQRankSum
type: SiteQuality
SIO_000300: -4.663e0

QD
type: SiteQuality
SIO_000300: 2.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.83e0

VQSLOD
type: SiteQuality
SIO_000300: -5.357e0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.25e1
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GenotypeQuality
all individuals: 8
bin: 4.25e1
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GenotypeQuality
all individuals: 10
bin: 4.75e1
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GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.818622696411251e-4
allele num: 16496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 10358
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66502
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.806e1

VQSLOD
type: SiteQuality
SIO_000300: -2.446e0

MQRankSum
type: SiteQuality
SIO_000300: 4.24e-1

QD
type: SiteQuality
SIO_000300: 1.432e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.215e0

FS
type: SiteQuality
SIO_000300: 1.097e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 6.712074e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

GenotypeQuality
all individuals: 602
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51393
bin: 9.75e1
variant carriers: 5

South Asian
type: Population
allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.017571308220002e-5
allele num: 66472
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.143e0

DP
type: SiteQuality
SIO_000300: 6.711408e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.818e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.16e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.07e0

MQRankSum
type: SiteQuality
SIO_000300: -3.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

QD
type: SiteQuality
SIO_000300: 9.06e0

GenotypeQuality
all individuals: 327
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51392
bin: 9.75e1
variant carriers: 8

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: 10340
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 8
allele frequency: 6.91323885240235e-4
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.762e0

VQSLOD
type: SiteQuality
SIO_000300: -1.766e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.831e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.841e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 6.709743e6

QD
type: SiteQuality
SIO_000300: 1.301e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4096
bin: 6.25e1
variant carriers: 0

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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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 914
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 6.668283220174588e-4
allele num: 16496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66382
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.183e0

DP
type: SiteQuality
SIO_000300: 6.711128e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.68e-1

MQ
type: SiteQuality
SIO_000300: 5.797e1

VQSLOD
type: SiteQuality
SIO_000300: -1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e-1

QD
type: SiteQuality
SIO_000300: 1.282e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.76e0

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

GenotypeQuality
all individuals: 306
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 51384
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 3.25e1
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GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 913
bin: 7.75e1
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GenotypeQuality
all individuals: 73
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1531
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66402
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

VQSLOD
type: SiteQuality
SIO_000300: -1.819e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.06e0

DP
type: SiteQuality
SIO_000300: 6.704604e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.81e-1

FS
type: SiteQuality
SIO_000300: 1.047e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.36e0

QD
type: SiteQuality
SIO_000300: 1.28e1

MQ
type: SiteQuality
SIO_000300: 5.746e1

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

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1531
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
all individuals: 494
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GenotypeQuality
all individuals: 668
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GenotypeQuality
all individuals: 45
bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 914
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51384
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 329
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66406
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 6.704479e6

MQ
type: SiteQuality
SIO_000300: 5.859e1

QD
type: SiteQuality
SIO_000300: 1.133e1

MQRankSum
type: SiteQuality
SIO_000300: 1.52e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.355e0

FS
type: SiteQuality
SIO_000300: 6.505e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.282e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.023552088666687e-5
allele num: 66406
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.999e0

FS
type: SiteQuality
SIO_000300: 3.602e0

MQRankSum
type: SiteQuality
SIO_000300: 5.49e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.646e0

MQ
type: SiteQuality
SIO_000300: 5.83e1

DP
type: SiteQuality
SIO_000300: 6.704763e6

QD
type: SiteQuality
SIO_000300: 1.16e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.53e-1

GenotypeQuality
all individuals: 129
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 5.25e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
all individuals: 120
bin: 2.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 66386
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.04e0

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

MQ
type: SiteQuality
SIO_000300: 5.866e1

VQSLOD
type: SiteQuality
SIO_000300: -1.866e0

QD
type: SiteQuality
SIO_000300: 1.091e1

DP
type: SiteQuality
SIO_000300: 6.703822e6

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 493
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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: 602
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variant carriers: 0

GenotypeQuality
all individuals: 51383
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66386
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 10336
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.866e1

DP
type: SiteQuality
SIO_000300: 6.703822e6

MQRankSum
type: SiteQuality
SIO_000300: 2.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.43e-1

FS
type: SiteQuality
SIO_000300: 1.864e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

VQSLOD
type: SiteQuality
SIO_000300: -1.866e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
SIO_000300: 1.091e1

GenotypeQuality
all individuals: 493
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
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GenotypeQuality
all individuals: 29
bin: 4.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 7.5e0
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GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51384
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.21300339640951e-4
allele num: 16488
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: 5
allele frequency: 4.838397522740468e-4
allele num: 10334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 6.703869e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.303e0

QD
type: SiteQuality
SIO_000300: 1.114e1

MQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.158e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

MQ
type: SiteQuality
SIO_000300: 5.834e1

GenotypeQuality
all individuals: 3855
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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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variant carriers: 0

GenotypeQuality
all individuals: 328
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GenotypeQuality
all individuals: 658
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variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
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: 16486
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.816e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

QD
type: SiteQuality
SIO_000300: 1.225e1

VQSLOD
type: SiteQuality
SIO_000300: -1.843e0

FS
type: SiteQuality
SIO_000300: 5.324e0

DP
type: SiteQuality
SIO_000300: 6.702297e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.953e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.81e-1

GenotypeQuality
all individuals: 357
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 491
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variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 596
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variant carriers: 0

GenotypeQuality
all individuals: 900
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variant carriers: 0

GenotypeQuality
all individuals: 70
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variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51381
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 647
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507204437209863e-5
allele num: 66348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.347e1

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.649999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.302e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.92e0

MQ
type: SiteQuality
SIO_000300: 5.908e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

DP
type: SiteQuality
SIO_000300: 6.698616e6

GenotypeQuality
all individuals: 179
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 889
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 325
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variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 65
bin: 7.5e0
variant carriers: 4

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 279
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51344
bin: 9.75e1
variant carriers: 151

GenotypeQuality
all individuals: 593
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 119
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 369
bin: 2.25e1
variant carriers: 1

Other
type: Population
allele count: 1
allele frequency: 1.116071428571429e-3
allele num: 896
num of homozygotes: 0

Latino
type: Population
allele count: 13
allele frequency: 1.124178484953303e-3
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.903600464576074e-4
allele num: 10332
num of homozygotes: 0

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

South Asian
type: Population
allele count: 9
allele frequency: 5.462490895848507e-4
allele num: 16476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 146
allele frequency: 2.20211161387632e-3
allele num: 66300
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.758e0

VQSLOD
type: SiteQuality
SIO_000300: -6.359e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e0

MQRankSum
type: SiteQuality
SIO_000300: -4.593e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.343e0

DP
type: SiteQuality
SIO_000300: 6.708915e6

MQ
type: SiteQuality
SIO_000300: 5.661e1

QD
type: SiteQuality
SIO_000300: 1.81e0

GenotypeQuality
all individuals: 489
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 367
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variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 1387
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GenotypeQuality
all individuals: 139
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variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 635
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variant carriers: 0

GenotypeQuality
all individuals: 884
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GenotypeQuality
all individuals: 593
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51396
bin: 9.75e1
variant carriers: 5

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66324
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.427773731488225e-4
allele num: 16476
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.331e0

MQ
type: SiteQuality
SIO_000300: 5.835e1

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

DP
type: SiteQuality
SIO_000300: 6.701486e6

FS
type: SiteQuality
SIO_000300: 6.26e-1

QD
type: SiteQuality
SIO_000300: 1.311e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.842e0

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

GenotypeQuality
all individuals: 372
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 7.5e0
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GenotypeQuality
all individuals: 1381
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variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
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variant carriers: 0

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51400
bin: 9.75e1
variant carriers: 72

Other
type: Population
allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.070171178827243e-5
allele num: 16474
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 67
allele frequency: 6.4847077042199e-3
allele num: 10332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 1.507613447911955e-5
allele num: 66330
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e0

DP
type: SiteQuality
SIO_000300: 6.702772e6

FS
type: SiteQuality
SIO_000300: 6.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

QD
type: SiteQuality
SIO_000300: 1.208e1

VQSLOD
type: SiteQuality
SIO_000300: 8.699999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.807e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.28e-1

GenotypeQuality
all individuals: 273
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
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variant carriers: 0

GenotypeQuality
all individuals: 323
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GenotypeQuality
all individuals: 130
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GenotypeQuality
all individuals: 381
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variant carriers: 0

GenotypeQuality
all individuals: 489
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GenotypeQuality
all individuals: 158
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51390
bin: 9.75e1
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GenotypeQuality
all individuals: 877
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.678668215253581e-5
allele num: 10332
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
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: 66332
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.700511e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.53e-1

MQ
type: SiteQuality
SIO_000300: 5.8e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.51e-1

FS
type: SiteQuality
SIO_000300: 6.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.02e0

QD
type: SiteQuality
SIO_000300: 1.075e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.459e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.41e-1

GenotypeQuality
all individuals: 3085
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 343
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 205
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GenotypeQuality
all individuals: 321
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GenotypeQuality
all individuals: 489
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GenotypeQuality
all individuals: 233
bin: 4.75e1
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GenotypeQuality
all individuals: 1275
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GenotypeQuality
all individuals: 51390
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GenotypeQuality
all individuals: 150
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 869
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 7.25e1
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: 1
allele frequency: 9.68429207824908e-5
allele num: 10326
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 16480
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66334
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.01e-1

DP
type: SiteQuality
SIO_000300: 6.698325e6

FS
type: SiteQuality
SIO_000300: 8.712e0

MQRankSum
type: SiteQuality
SIO_000300: 7.54e0

MQ
type: SiteQuality
SIO_000300: 5.887e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

QD
type: SiteQuality
SIO_000300: 1.668e1

VQSLOD
type: SiteQuality
SIO_000300: 2.9e-2

GenotypeQuality
all individuals: 69
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
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GenotypeQuality
all individuals: 389
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 598
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GenotypeQuality
all individuals: 2221
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GenotypeQuality
all individuals: 851
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GenotypeQuality
all individuals: 51384
bin: 9.75e1
variant carriers: 202

GenotypeQuality
all individuals: 529
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 211
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 445
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1147
bin: 6.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 171
allele frequency: 2.580430977243918e-3
allele num: 66268
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 7.292173067574137e-4
allele num: 16456
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.876720294630742e-4
allele num: 10318
num of homozygotes: 0

Latino
type: Population
allele count: 21
allele frequency: 1.815038893690579e-3
allele num: 11570
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.378e0

MQ
type: SiteQuality
SIO_000300: 5.637e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e0

MQRankSum
type: SiteQuality
SIO_000300: -4.939e0

QD
type: SiteQuality
SIO_000300: 2.82e0

VQSLOD
type: SiteQuality
SIO_000300: -4.623e0

DP
type: SiteQuality
SIO_000300: 6.696516e6

GenotypeQuality
all individuals: 240
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7303
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4609
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3342
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18825
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2437
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7256
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 1.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14950
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.54642417612471e-5
allele num: 58504
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.083893344894862e-4
allele num: 9226
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9634
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5858
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

DP
type: SiteQuality
SIO_000300: 1.070466e6

MQ
type: SiteQuality
SIO_000300: 5.936e1

FS
type: SiteQuality
SIO_000300: 2.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.12e-1

QD
type: SiteQuality
SIO_000300: 1.087e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

GenotypeQuality
all individuals: 405
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7515
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7174
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2868
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6856
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21539
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 503
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5848
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9254
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9642
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.280081925243216e-4
allele num: 7812
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 3.762e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.835e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.938e-1

QD
type: SiteQuality
SIO_000300: 1.053e1

DP
type: SiteQuality
SIO_000300: 1.09056e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.529e0

GenotypeQuality
all individuals: 7071
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 606
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2646
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1254
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7580
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2895
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14980
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7854
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58674
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5870
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.07828337287039e-4
allele num: 9274
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.798e1

MQRankSum
type: SiteQuality
SIO_000300: 9.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.23e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.893e0

DP
type: SiteQuality
SIO_000300: 1.100139e6

QD
type: SiteQuality
SIO_000300: 1.818e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e0

GenotypeQuality
all individuals: 5990
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27356
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1752
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2574
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4854
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 275
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1661
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5924
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9810
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.640106241699867e-5
allele num: 15060
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59228
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7918
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9344
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.864e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.14e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.098e0

DP
type: SiteQuality
SIO_000300: 1.157253e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.331e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

MQRankSum
type: SiteQuality
SIO_000300: -1.866e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

GenotypeQuality
all individuals: 2635
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3401
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1550
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30491
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1212
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5585
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 9.75e1
variant carriers: 15

East Asian
type: Population
allele count: 16
allele frequency: 2.014098690835851e-3
allele num: 7944
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5938
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59460
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15138
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.89e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

QD
type: SiteQuality
SIO_000300: 1.322e1

DP
type: SiteQuality
SIO_000300: 1.17701e6

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 231
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 113
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1408
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7011
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4117
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1208
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2676
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1397
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 9.75e1
variant carriers: 176

European (Non-Finnish)
type: Population
allele count: 154
allele frequency: 2.579391665550047e-3
allele num: 59704
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15162
num of homozygotes: 0

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

African
type: Population
allele count: 6
allele frequency: 6.389776357827476e-4
allele num: 9390
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 1.210409521888239e-3
allele num: 9914
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 1.008403361344538e-3
allele num: 5950
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.75e0

QD
type: SiteQuality
SIO_000300: 1.316e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.185353e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

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

GenotypeQuality
all individuals: 1163
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3102
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 97
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2761
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3614
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9970
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.589351607801793e-5
allele num: 15176
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8024
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60002
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5972
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9412
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

MQ
type: SiteQuality
SIO_000300: 5.896e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

QD
type: SiteQuality
SIO_000300: 1.108e1

DP
type: SiteQuality
SIO_000300: 1.202741e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

FS
type: SiteQuality
SIO_000300: 5.714e0

GenotypeQuality
all individuals: 6784
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 110
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3614
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4908
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2761
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3102
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.246261216350947e-4
allele num: 8024
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60002
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9970
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15176
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5972
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

QD
type: SiteQuality
SIO_000300: 1.108e1

DP
type: SiteQuality
SIO_000300: 1.202741e6

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

FS
type: SiteQuality
SIO_000300: 5.714e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

MQ
type: SiteQuality
SIO_000300: 5.896e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.28e-1

GenotypeQuality
all individuals: 3102
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33654
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3614
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 392
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 2761
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4908
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60002
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9970
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8024
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.317870321560359e-4
allele num: 15176
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5972
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.108e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

DP
type: SiteQuality
SIO_000300: 1.202741e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

FS
type: SiteQuality
SIO_000300: 5.714e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.28e-1

MQ
type: SiteQuality
SIO_000300: 5.896e1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0