6-84265830-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265830
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265830
    reference: chr 6
allele count: 1
allele frequency: 4.553734061930783e-5
allele num: 21960
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.*10+32G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.*10+32G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.*10+32G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.*10+32G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.*10+32G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.*10+32G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.*10+32G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.*10+32G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2444+32G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.*10+32G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1826G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2825+32G>A
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-84265835-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265835
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265835
    reference: chr 6
allele count: 1
allele frequency: 4.528165187466039e-5
allele num: 22084
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.*10+27G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.*10+27G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.*10+27G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.*10+27G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2825+27G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2444+27G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.*10+27G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1831G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.*10+27G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.*10+27G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.*10+27G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.*10+27G>A
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35806
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

6-84265852-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265852
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265852
    reference: chr 6
allele count: 1
allele frequency: 4.459109961651654e-5
allele num: 22426
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.*10+10A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1848A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2444+10A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.*10+10A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.*10+10A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.*10+10A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.*10+10A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.*10+10A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.*10+10A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2825+10A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.*10+10A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.*10+10A>G
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34648
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD

6-84265855-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265855
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265855
    reference: chr 6
allele count: 1
allele frequency: 4.444049417829526e-5
allele num: 22502
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.*10+7A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.*10+7A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.*10+7A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.*10+7A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.*10+7A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2444+7A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2825+7A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.*10+7A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.*10+7A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.*10+7A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.*10+7A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1851A>T
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34038
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*10+7A>T
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

6-84265869-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265869
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265869
    reference: chr 6
allele count: 1
allele frequency: 4.29774798005845e-5
allele num: 23268
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.*3A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.*3A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.*3A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.*3A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.*3A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.*3A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.*3A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.*3A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2437A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1865A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2818A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.*3A>T
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16441
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29444
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

6-84265875-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265875
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265875
    reference: chr 6
allele count: 14
allele frequency: 5.890768324497181e-4
allele num: 23766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2431G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1800G>A
  hgvsp: ENST00000437520.1:c.1800G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2721G>A
  hgvsp: ENST00000521743.1:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2706G>A
  hgvsp: ENST00000195649.6:c.2706G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2631G>A
  hgvsp: ENST00000520302.1:c.2631G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1800G>A
  hgvsp: ENST00000520213.1:c.1800G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2721G>A
  hgvsp: ENST00000369694.2:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2706G>A
  hgvsp: ENST00000521485.1:c.2706G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2812G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2721G>A
  hgvsp: ENST00000428679.2:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2721G>A
  hgvsp: ENST00000439399.2:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1871G>A
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26435
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu907Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD

6-84265883-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265883
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265883
    reference: chr 6
allele count: 1
allele frequency: 4.067355405515334e-5
allele num: 24586
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2713G>A
  hgvsp: ENSP00000358708.2:p.Asp905Asn
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2713G>A
  hgvsp: ENSP00000400459.2:p.Asp905Asn
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2804G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2698G>A
  hgvsp: ENSP00000429776.1:p.Asp900Asn
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2713G>A
  hgvsp: ENSP00000412492.2:p.Asp905Asn
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1792G>A
  hgvsp: ENSP00000428026.1:p.Asp598Asn
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1879G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2423G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2713G>A
  hgvsp: ENSP00000428215.1:p.Asp905Asn
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2623G>A
  hgvsp: ENSP00000428511.1:p.Asp875Asn
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2698G>A
  hgvsp: ENSP00000195649.6:p.Asp900Asn
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1792G>A
  hgvsp: ENSP00000413277.1:p.Asp598Asn
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24025
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22473
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp905Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

6-84265899-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265899
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265899
    reference: chr 6
allele count: 7
allele frequency: 2.620937546802456e-4
allele num: 26708
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1895G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2682G>A
  hgvsp: ENST00000195649.6:c.2682G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1776G>A
  hgvsp: ENST00000437520.1:c.1776G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2697G>A
  hgvsp: ENST00000439399.2:c.2697G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2607G>A
  hgvsp: ENST00000520302.1:c.2607G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2697G>A
  hgvsp: ENST00000428679.2:c.2697G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2407G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2697G>A
  hgvsp: ENST00000521743.1:c.2697G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2697G>A
  hgvsp: ENST00000369694.2:c.2697G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2788G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2682G>A
  hgvsp: ENST00000521485.1:c.2682G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1776G>A
  hgvsp: ENST00000520213.1:c.1776G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16341
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29632
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala899Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-84265900-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265900
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265900
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 27012
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1775C>T
  hgvsp: ENSP00000413277.1:p.Ala592Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2681C>T
  hgvsp: ENSP00000429776.1:p.Ala894Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2606C>T
  hgvsp: ENSP00000428511.1:p.Ala869Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2696C>T
  hgvsp: ENSP00000400459.2:p.Ala899Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2696C>T
  hgvsp: ENSP00000358708.2:p.Ala899Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1896C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2696C>T
  hgvsp: ENSP00000428215.1:p.Ala899Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1775C>T
  hgvsp: ENSP00000428026.1:p.Ala592Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2696C>T
  hgvsp: ENSP00000412492.2:p.Ala899Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2406C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2681C>T
  hgvsp: ENSP00000195649.6:p.Ala894Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2787C>T
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15981
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29888
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala899Val
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-84265905-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265905
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265905
    reference: chr 6
allele count: 2
allele frequency: 7.192692224699705e-5
allele num: 27806
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2782A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2691A>G
  hgvsp: ENST00000439399.2:c.2691A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2401A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2601A>G
  hgvsp: ENST00000520302.1:c.2601A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2691A>G
  hgvsp: ENST00000369694.2:c.2691A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2691A>G
  hgvsp: ENST00000521743.1:c.2691A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1770A>G
  hgvsp: ENST00000520213.1:c.1770A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2676A>G
  hgvsp: ENST00000195649.6:c.2676A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1770A>G
  hgvsp: ENST00000437520.1:c.1770A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1901A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2691A>G
  hgvsp: ENST00000428679.2:c.2691A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2676A>G
  hgvsp: ENST00000521485.1:c.2676A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14878
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro897Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-84265914-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265914
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265914
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 29052
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2682A>G
  hgvsp: ENST00000369694.2:c.2682A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2682A>G
  hgvsp: ENST00000439399.2:c.2682A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1761A>G
  hgvsp: ENST00000520213.1:c.1761A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2667A>G
  hgvsp: ENST00000195649.6:c.2667A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2592A>G
  hgvsp: ENST00000520302.1:c.2592A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2682A>G
  hgvsp: ENST00000521743.1:c.2682A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2682A>G
  hgvsp: ENST00000428679.2:c.2682A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2773A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2667A>G
  hgvsp: ENST00000521485.1:c.2667A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1761A>G
  hgvsp: ENST00000437520.1:c.1761A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1910A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2392A>G
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13779
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31366
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6083
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala894Ala
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

6-84265915-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265915
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265915
    reference: chr 6
allele count: 1
allele frequency: 3.43218012081274e-5
allele num: 29136
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2681C>A
  hgvsp: ENSP00000412492.2:p.Ala894Glu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2666C>A
  hgvsp: ENSP00000429776.1:p.Ala889Glu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2591C>A
  hgvsp: ENSP00000428511.1:p.Ala864Glu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2681C>A
  hgvsp: ENSP00000400459.2:p.Ala894Glu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1911C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2681C>A
  hgvsp: ENSP00000358708.2:p.Ala894Glu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2666C>A
  hgvsp: ENSP00000195649.6:p.Ala889Glu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1760C>A
  hgvsp: ENSP00000413277.1:p.Ala587Glu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2772C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2681C>A
  hgvsp: ENSP00000428215.1:p.Ala894Glu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1760C>A
  hgvsp: ENSP00000428026.1:p.Ala587Glu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2391C>A
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13582
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala894Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-84265921-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265921
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265921
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 29746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2675C>T
  hgvsp: ENSP00000358708.2:p.Pro892Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2675C>T
  hgvsp: ENSP00000428215.1:p.Pro892Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2675C>T
  hgvsp: ENSP00000412492.2:p.Pro892Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1754C>T
  hgvsp: ENSP00000413277.1:p.Pro585Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2585C>T
  hgvsp: ENSP00000428511.1:p.Pro862Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2660C>T
  hgvsp: ENSP00000195649.6:p.Pro887Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1754C>T
  hgvsp: ENSP00000428026.1:p.Pro585Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2675C>T
  hgvsp: ENSP00000400459.2:p.Pro892Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2766C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2660C>T
  hgvsp: ENSP00000429776.1:p.Pro887Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2385C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1917C>T
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13403
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31318
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro892Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ

6-84265925-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265925
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265925
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 29930
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2581A>C
  hgvsp: ENSP00000428511.1:p.Lys861Gln
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2656A>C
  hgvsp: ENSP00000429776.1:p.Lys886Gln
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1750A>C
  hgvsp: ENSP00000428026.1:p.Lys584Gln
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1750A>C
  hgvsp: ENSP00000413277.1:p.Lys584Gln
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2671A>C
  hgvsp: ENSP00000428215.1:p.Lys891Gln
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2381A>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2671A>C
  hgvsp: ENSP00000358708.2:p.Lys891Gln
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2671A>C
  hgvsp: ENSP00000400459.2:p.Lys891Gln
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2656A>C
  hgvsp: ENSP00000195649.6:p.Lys886Gln
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2762A>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2671A>C
  hgvsp: ENSP00000412492.2:p.Lys891Gln
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1921A>C
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13674
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30957
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys891Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

6-84265935-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265935
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265936
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 30232
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2660dupA
  hgvsp: ENSP00000428215.1:p.Ser888GlufsTer15
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2660dupA
  hgvsp: ENSP00000412492.2:p.Ser888GlufsTer15
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2645dupA
  hgvsp: ENSP00000195649.6:p.Ser883GlufsTer15
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2570dupA
  hgvsp: ENSP00000428511.1:p.Ser858GlufsTer15
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2660dupA
  hgvsp: ENSP00000358708.2:p.Ser888GlufsTer15
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2645dupA
  hgvsp: ENSP00000429776.1:p.Ser883GlufsTer15
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1739dupA
  hgvsp: ENSP00000413277.1:p.Ser581GlufsTer15
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2660dupA
  hgvsp: ENSP00000400459.2:p.Ser888GlufsTer15
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1739dupA
  hgvsp: ENSP00000428026.1:p.Ser581GlufsTer15
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2751dupA
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1932dupA
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2370dupA
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: frameshift
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 14578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29716
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser888GlufsTer15
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/6-84265943-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265943
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265943
    reference: chr 6
allele count: 1
allele frequency: 3.354579000335458e-5
allele num: 29810
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2653G>T
  hgvsp: ENSP00000428215.1:p.Ala885Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2563G>T
  hgvsp: ENSP00000428511.1:p.Ala855Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2653G>T
  hgvsp: ENSP00000400459.2:p.Ala885Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1732G>T
  hgvsp: ENSP00000428026.1:p.Ala578Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1939G>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2653G>T
  hgvsp: ENSP00000358708.2:p.Ala885Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2638G>T
  hgvsp: ENSP00000195649.6:p.Ala880Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2363G>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2653G>T
  hgvsp: ENSP00000412492.2:p.Ala885Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1732G>T
  hgvsp: ENSP00000413277.1:p.Ala578Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2744G>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2638G>T
  hgvsp: ENSP00000429776.1:p.Ala880Ser
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27106
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16971
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala885Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

6-84265945-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265945
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265945
    reference: chr 6
allele count: 1
allele frequency: 3.359989248034406e-5
allele num: 29762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2651C>A
  hgvsp: ENSP00000358708.2:p.Pro884His
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2361C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1941C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2561C>A
  hgvsp: ENSP00000428511.1:p.Pro854His
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2742C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1730C>A
  hgvsp: ENSP00000413277.1:p.Pro577His
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2636C>A
  hgvsp: ENSP00000429776.1:p.Pro879His
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2636C>A
  hgvsp: ENSP00000195649.6:p.Pro879His
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1730C>A
  hgvsp: ENSP00000428026.1:p.Pro577His
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2651C>A
  hgvsp: ENSP00000428215.1:p.Pro884His
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2651C>A
  hgvsp: ENSP00000400459.2:p.Pro884His
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2651C>A
  hgvsp: ENSP00000412492.2:p.Pro884His
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26526
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17601
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro884His
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

6-84265947-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265947
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265947
    reference: chr 6
allele count: 21
allele frequency: 7.699076110866696e-4
allele num: 27276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1728A>C
  hgvsp: ENST00000520213.1:c.1728A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2634A>C
  hgvsp: ENST00000521485.1:c.2634A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2649A>C
  hgvsp: ENST00000428679.2:c.2649A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1728A>C
  hgvsp: ENST00000437520.1:c.1728A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2649A>C
  hgvsp: ENST00000521743.1:c.2649A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2740A>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2649A>C
  hgvsp: ENST00000369694.2:c.2649A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2649A>C
  hgvsp: ENST00000439399.2:c.2649A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1943A>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2559A>C
  hgvsp: ENST00000520302.1:c.2559A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2634A>C
  hgvsp: ENST00000195649.6:c.2634A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2359A>C
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 25004
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18721
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Thr883Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

6-84265952-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265952
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265952
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 28802
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2629C>G
  hgvsp: ENSP00000429776.1:p.Pro877Ala
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2644C>G
  hgvsp: ENSP00000358708.2:p.Pro882Ala
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1723C>G
  hgvsp: ENSP00000428026.1:p.Pro575Ala
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2354C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1723C>G
  hgvsp: ENSP00000413277.1:p.Pro575Ala
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1948C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2644C>G
  hgvsp: ENSP00000412492.2:p.Pro882Ala
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2735C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2644C>G
  hgvsp: ENSP00000428215.1:p.Pro882Ala
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2629C>G
  hgvsp: ENSP00000195649.6:p.Pro877Ala
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2644C>G
  hgvsp: ENSP00000400459.2:p.Pro882Ala
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2554C>G
  hgvsp: ENSP00000428511.1:p.Pro852Ala
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23936
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20458
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro882Ala
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

6-84265954-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265954
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265954
    reference: chr 6
allele count: 1
allele frequency: 3.507049168829347e-5
allele num: 28514
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2552G>A
  hgvsp: ENSP00000428511.1:p.Ser851Asn
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2627G>A
  hgvsp: ENSP00000429776.1:p.Ser876Asn
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2627G>A
  hgvsp: ENSP00000195649.6:p.Ser876Asn
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2642G>A
  hgvsp: ENSP00000428215.1:p.Ser881Asn
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1950G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1721G>A
  hgvsp: ENSP00000428026.1:p.Ser574Asn
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2352G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2642G>A
  hgvsp: ENSP00000412492.2:p.Ser881Asn
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2733G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1721G>A
  hgvsp: ENSP00000413277.1:p.Ser574Asn
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2642G>A
  hgvsp: ENSP00000358708.2:p.Ser881Asn
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2642G>A
  hgvsp: ENSP00000400459.2:p.Ser881Asn
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23206
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser881Asn
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

6-84265958-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265958
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265958
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 28086
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2623C>G
  hgvsp: ENSP00000429776.1:p.Pro875Ala
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1717C>G
  hgvsp: ENSP00000413277.1:p.Pro573Ala
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2729C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2638C>G
  hgvsp: ENSP00000400459.2:p.Pro880Ala
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2638C>G
  hgvsp: ENSP00000428215.1:p.Pro880Ala
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2638C>G
  hgvsp: ENSP00000358708.2:p.Pro880Ala
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2623C>G
  hgvsp: ENSP00000195649.6:p.Pro875Ala
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1954C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2638C>G
  hgvsp: ENSP00000412492.2:p.Pro880Ala
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1717C>G
  hgvsp: ENSP00000428026.1:p.Pro573Ala
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2548C>G
  hgvsp: ENSP00000428511.1:p.Pro850Ala
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2348C>G
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 22596
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21840
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro880Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-84265967-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265967
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265967
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 27082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2632-3T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2632-3T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2723-3T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2617-3T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2617-3T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1711-3T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2632-3T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2632-3T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2342-3T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1711-3T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1963T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2542-3T>C
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17798
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26505
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2632-3T>C
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

6-84265987-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265987
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265987
    reference: chr 6
allele count: 1
allele frequency: 4.183400267737617e-5
allele num: 23904
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2342-23T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2632-23T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2723-23T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2617-23T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2632-23T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2632-23T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2617-23T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1983T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1711-23T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2542-23T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1711-23T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2632-23T>C
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9832
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS

6-84265993-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84265993
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84265993
    reference: chr 6
allele count: 2
allele frequency: 8.60141063134354e-5
allele num: 23252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1989G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2542-29G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2723-29G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1711-29G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2617-29G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1711-29G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2632-29G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2617-29G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2632-29G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2632-29G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2342-29G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2632-29G>A
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33523
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8842
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum

6-84266001-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84266001
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84266001
    reference: chr 6
allele count: 19
allele frequency: 8.548546747053001e-4
allele num: 22226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.655-1997C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2617-37C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2723-37C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2542-37C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1711-37C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2632-37C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2342-37C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2617-37C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2632-37C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2632-37C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2632-37C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1711-37C>G
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32833
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8038
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

6-84269777-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269777
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269777
    reference: chr 6
allele count: 1
allele frequency: 8.341396683460679e-6
allele num: 119884
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2631+46T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2631+46T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2631+46T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2722+46T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2541+46T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2616+46T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.654+46T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2631+46T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1710+46T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1710+46T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2616+46T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2341+46T>C
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3686
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

6-84269778-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269778
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269778
    reference: chr 6
allele count: 1
allele frequency: 8.344459279038718e-6
allele num: 119840
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2616+45G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2631+45G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1710+45G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2722+45G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2541+45G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.654+45G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2341+45G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2631+45G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2616+45G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2631+45G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2631+45G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1710+45G>A
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

6-84269778-CTTATTAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269778
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269771
    reference: chr 6
allele count: 1
allele frequency: 8.344459279038718e-6
allele num: 119840
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.654+38_654+44delCTAATAA
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2631+38_2631+44delCTAATAA
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1710+38_1710+44delCTAATAA
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2631+38_2631+44delCTAATAA
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2616+38_2616+44delCTAATAA
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2616+38_2616+44delCTAATAA
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2631+38_2631+44delCTAATAA
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2631+38_2631+44delCTAATAA
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2722+38_*2722+44delCTAATAA
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2341+38_*2341+44delCTAATAA
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2541+38_2541+44delCTAATAA
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1710+38_1710+44delCTAATAA
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: CTTATTAG
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum

6-84269784-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269784
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269784
    reference: chr 6
allele count: 1
allele frequency: 8.340283569641367e-6
allele num: 119900
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2631+39T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2722+39T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.654+39T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1710+39T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2616+39T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1710+39T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2541+39T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2616+39T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2631+39T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2631+39T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2631+39T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2341+39T>C
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3335
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-84269790-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269790
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269790
    reference: chr 6
allele count: 3
allele frequency: 2.499958334027766e-5
allele num: 120002
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2631+33A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2616+33A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2631+33A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2631+33A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2631+33A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2341+33A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.654+33A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1710+33A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2616+33A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2722+33A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2541+33A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1710+33A>G
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11543
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14505
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

6-84269795-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269795
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269795
    reference: chr 6
allele count: 2
allele frequency: 1.665278934221482e-5
allele num: 120100
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2722+28G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2631+28G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2616+28G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2616+28G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1710+28G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2631+28G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2631+28G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2541+28G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2631+28G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2341+28G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.654+28G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1710+28G>A
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5903
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14901
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

6-84269801-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269801
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269801
    reference: chr 6
allele count: 1
allele frequency: 8.318221896887321e-6
allele num: 120218
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1710+22A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1710+22A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2541+22A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2631+22A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.654+22A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2722+22A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2631+22A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2631+22A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2616+22A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2631+22A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2616+22A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2341+22A>G
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

6-84269809-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269809
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269809
    reference: chr 6
allele count: 1
allele frequency: 8.311032063961702e-6
allele num: 120322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2616+14A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1710+14A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.654+14A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2631+14A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2631+14A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2616+14A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2631+14A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2541+14A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2722+14A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2341+14A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2631+14A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1710+14A>G
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18250
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5903
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15063
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/6-84269812-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269812
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269812
    reference: chr 6
allele count: 1
allele frequency: 8.30675172780436e-6
allele num: 120384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2631+11T>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2616+11T>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2616+11T>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.654+11T>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2722+11T>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2631+11T>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2341+11T>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2631+11T>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1710+11T>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2631+11T>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2541+11T>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1710+11T>G
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/6-84269826-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269826
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269826
    reference: chr 6
allele count: 4
allele frequency: 3.318951211417192e-5
allele num: 120520
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2338G>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2613G>T
  hgvsp: ENST00000195649.6:c.2613G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1707G>T
  hgvsp: ENST00000520213.1:c.1707G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2538G>T
  hgvsp: ENST00000520302.1:c.2538G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2719G>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2628G>T
  hgvsp: ENST00000439399.2:c.2628G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2628G>T
  hgvsp: ENST00000369694.2:c.2628G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2628G>T
  hgvsp: ENST00000428679.2:c.2628G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2628G>T
  hgvsp: ENST00000521743.1:c.2628G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1707G>T
  hgvsp: ENST00000437520.1:c.1707G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2613G>T
  hgvsp: ENST00000521485.1:c.2613G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.651G>T
  hgvsp: ENST00000523448.1:c.651G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5904
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr876Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

6-84269826-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269826
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269826
    reference: chr 6
allele count: 10
allele frequency: 8.297378028542981e-5
allele num: 120520
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1707G>A
  hgvsp: ENST00000437520.1:c.1707G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2628G>A
  hgvsp: ENST00000521743.1:c.2628G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2538G>A
  hgvsp: ENST00000520302.1:c.2538G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2628G>A
  hgvsp: ENST00000439399.2:c.2628G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1707G>A
  hgvsp: ENST00000520213.1:c.1707G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2613G>A
  hgvsp: ENST00000195649.6:c.2613G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2628G>A
  hgvsp: ENST00000369694.2:c.2628G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2613G>A
  hgvsp: ENST00000521485.1:c.2613G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2338G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.651G>A
  hgvsp: ENST00000523448.1:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2628G>A
  hgvsp: ENST00000428679.2:c.2628G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2719G>A
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5904
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr876Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

6-84269827-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269827
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269827
    reference: chr 6
allele count: 6
allele frequency: 4.977765978628792e-5
allele num: 120536
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2627C>T
  hgvsp: ENSP00000428215.1:p.Thr876Met
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2627C>T
  hgvsp: ENSP00000358708.2:p.Thr876Met
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2627C>T
  hgvsp: ENSP00000400459.2:p.Thr876Met
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1706C>T
  hgvsp: ENSP00000428026.1:p.Thr569Met
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2718C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2537C>T
  hgvsp: ENSP00000428511.1:p.Thr846Met
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2612C>T
  hgvsp: ENSP00000195649.6:p.Thr871Met
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.650C>T
  hgvsp: ENSP00000430255.1:p.Thr217Met
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1706C>T
  hgvsp: ENSP00000413277.1:p.Thr569Met
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2612C>T
  hgvsp: ENSP00000429776.1:p.Thr871Met
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2337C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2627C>T
  hgvsp: ENSP00000412492.2:p.Thr876Met
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr876Met
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

6-84269833-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269833
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269833
    reference: chr 6
allele count: 4
allele frequency: 3.318015163329296e-5
allele num: 120554
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2621C>T
  hgvsp: ENSP00000412492.2:p.Pro874Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2621C>T
  hgvsp: ENSP00000358708.2:p.Pro874Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2331C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2621C>T
  hgvsp: ENSP00000400459.2:p.Pro874Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1700C>T
  hgvsp: ENSP00000413277.1:p.Pro567Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2621C>T
  hgvsp: ENSP00000428215.1:p.Pro874Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.644C>T
  hgvsp: ENSP00000430255.1:p.Pro215Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2606C>T
  hgvsp: ENSP00000429776.1:p.Pro869Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2531C>T
  hgvsp: ENSP00000428511.1:p.Pro844Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2712C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2606C>T
  hgvsp: ENSP00000195649.6:p.Pro869Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1700C>T
  hgvsp: ENSP00000428026.1:p.Pro567Leu
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5907
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18464
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro874Leu
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

6-84269839-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269839
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269839
    reference: chr 6
allele count: 8
allele frequency: 6.635479911084569e-5
allele num: 120564
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2615C>G
  hgvsp: ENSP00000400459.2:p.Ala872Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2615C>G
  hgvsp: ENSP00000358708.2:p.Ala872Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1694C>G
  hgvsp: ENSP00000428026.1:p.Ala565Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.638C>G
  hgvsp: ENSP00000430255.1:p.Ala213Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2600C>G
  hgvsp: ENSP00000429776.1:p.Ala867Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1694C>G
  hgvsp: ENSP00000413277.1:p.Ala565Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2615C>G
  hgvsp: ENSP00000412492.2:p.Ala872Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2615C>G
  hgvsp: ENSP00000428215.1:p.Ala872Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2325C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2706C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2525C>G
  hgvsp: ENSP00000428511.1:p.Ala842Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2600C>G
  hgvsp: ENSP00000195649.6:p.Ala867Gly
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5909
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11759
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala872Gly
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS

6-84269841-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269841
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269841
    reference: chr 6
allele count: 1
allele frequency: 8.294212298657997e-6
allele num: 120566
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2523C>T
  hgvsp: ENST00000520302.1:c.2523C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2598C>T
  hgvsp: ENST00000521485.1:c.2598C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2613C>T
  hgvsp: ENST00000521743.1:c.2613C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.636C>T
  hgvsp: ENST00000523448.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1692C>T
  hgvsp: ENST00000437520.1:c.1692C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2323C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2704C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2613C>T
  hgvsp: ENST00000369694.2:c.2613C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2598C>T
  hgvsp: ENST00000195649.6:c.2598C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2613C>T
  hgvsp: ENST00000428679.2:c.2613C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1692C>T
  hgvsp: ENST00000520213.1:c.1692C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2613C>T
  hgvsp: ENST00000439399.2:c.2613C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala871Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD

6-84269842-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269842
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269842
    reference: chr 6
allele count: 7
allele frequency: 5.805948609060597e-5
allele num: 120566
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.635C>T
  hgvsp: ENSP00000430255.1:p.Ala212Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2703C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2612C>T
  hgvsp: ENSP00000400459.2:p.Ala871Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2597C>T
  hgvsp: ENSP00000195649.6:p.Ala866Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1691C>T
  hgvsp: ENSP00000413277.1:p.Ala564Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2597C>T
  hgvsp: ENSP00000429776.1:p.Ala866Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2612C>T
  hgvsp: ENSP00000412492.2:p.Ala871Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2322C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2612C>T
  hgvsp: ENSP00000428215.1:p.Ala871Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2612C>T
  hgvsp: ENSP00000358708.2:p.Ala871Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1691C>T
  hgvsp: ENSP00000428026.1:p.Ala564Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2522C>T
  hgvsp: ENSP00000428511.1:p.Ala841Val
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5911
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala871Val
num of homozygotes: 1
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

6-84269856-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269856
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269856
    reference: chr 6
allele count: 1
allele frequency: 8.29228651508367e-6
allele num: 120594
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2583C>G
  hgvsp: ENST00000521485.1:c.2583C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2308C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1677C>G
  hgvsp: ENST00000520213.1:c.1677C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2598C>G
  hgvsp: ENST00000439399.2:c.2598C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1677C>G
  hgvsp: ENST00000437520.1:c.1677C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2689C>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2508C>G
  hgvsp: ENST00000520302.1:c.2508C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2583C>G
  hgvsp: ENST00000195649.6:c.2583C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.621C>G
  hgvsp: ENST00000523448.1:c.621C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2598C>G
  hgvsp: ENST00000369694.2:c.2598C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2598C>G
  hgvsp: ENST00000521743.1:c.2598C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2598C>G
  hgvsp: ENST00000428679.2:c.2598C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5916
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18548
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro866Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

6-84269865-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269865
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269865
    reference: chr 6
allele count: 4
allele frequency: 3.317354741329264e-5
allele num: 120578
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2589G>C
  hgvsp: ENSP00000428215.1:p.Met863Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2589G>C
  hgvsp: ENSP00000358708.2:p.Met863Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1668G>C
  hgvsp: ENSP00000413277.1:p.Met556Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2574G>C
  hgvsp: ENSP00000429776.1:p.Met858Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2680G>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2589G>C
  hgvsp: ENSP00000412492.2:p.Met863Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2589G>C
  hgvsp: ENSP00000400459.2:p.Met863Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2574G>C
  hgvsp: ENSP00000195649.6:p.Met858Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2299G>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.612G>C
  hgvsp: ENSP00000430255.1:p.Met204Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1668G>C
  hgvsp: ENSP00000428026.1:p.Met556Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2499G>C
  hgvsp: ENSP00000428511.1:p.Met833Ile
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met863Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-84269867-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269867
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269867
    reference: chr 6
allele count: 1
allele frequency: 8.293386853323161e-6
allele num: 120578
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2572A>G
  hgvsp: ENSP00000429776.1:p.Met858Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2587A>G
  hgvsp: ENSP00000358708.2:p.Met863Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2587A>G
  hgvsp: ENSP00000400459.2:p.Met863Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.610A>G
  hgvsp: ENSP00000430255.1:p.Met204Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2297A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2587A>G
  hgvsp: ENSP00000428215.1:p.Met863Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2572A>G
  hgvsp: ENSP00000195649.6:p.Met858Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2497A>G
  hgvsp: ENSP00000428511.1:p.Met833Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2587A>G
  hgvsp: ENSP00000412492.2:p.Met863Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1666A>G
  hgvsp: ENSP00000413277.1:p.Met556Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2678A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1666A>G
  hgvsp: ENSP00000428026.1:p.Met556Val
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11761
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met863Val
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

6-84269872-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269872
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269872
    reference: chr 6
allele count: 1
allele frequency: 8.294349888855711e-6
allele num: 120564
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2582A>G
  hgvsp: ENSP00000428215.1:p.Gln861Arg
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.605A>G
  hgvsp: ENSP00000430255.1:p.Gln202Arg
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2582A>G
  hgvsp: ENSP00000400459.2:p.Gln861Arg
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1661A>G
  hgvsp: ENSP00000413277.1:p.Gln554Arg
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2492A>G
  hgvsp: ENSP00000428511.1:p.Gln831Arg
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2567A>G
  hgvsp: ENSP00000195649.6:p.Gln856Arg
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2292A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2582A>G
  hgvsp: ENSP00000412492.2:p.Gln861Arg
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1661A>G
  hgvsp: ENSP00000428026.1:p.Gln554Arg
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2673A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2582A>G
  hgvsp: ENSP00000358708.2:p.Gln861Arg
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2567A>G
  hgvsp: ENSP00000429776.1:p.Gln856Arg
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln861Arg
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

6-84269875-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269875
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269875
    reference: chr 6
allele count: 4
allele frequency: 3.317794993447355e-5
allele num: 120562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2670C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2579C>T
  hgvsp: ENSP00000400459.2:p.Ala860Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1658C>T
  hgvsp: ENSP00000413277.1:p.Ala553Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2289C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2579C>T
  hgvsp: ENSP00000358708.2:p.Ala860Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2564C>T
  hgvsp: ENSP00000195649.6:p.Ala855Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2579C>T
  hgvsp: ENSP00000428215.1:p.Ala860Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1658C>T
  hgvsp: ENSP00000428026.1:p.Ala553Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2489C>T
  hgvsp: ENSP00000428511.1:p.Ala830Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.602C>T
  hgvsp: ENSP00000430255.1:p.Ala201Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2564C>T
  hgvsp: ENSP00000429776.1:p.Ala855Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2579C>T
  hgvsp: ENSP00000412492.2:p.Ala860Val
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11762
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala860Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

6-84269882-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269882
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269882
    reference: chr 6
allele count: 1
allele frequency: 8.296689620841284e-6
allele num: 120530
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2663A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1651A>G
  hgvsp: ENSP00000413277.1:p.Met551Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2557A>G
  hgvsp: ENSP00000429776.1:p.Met853Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1651A>G
  hgvsp: ENSP00000428026.1:p.Met551Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2572A>G
  hgvsp: ENSP00000358708.2:p.Met858Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2572A>G
  hgvsp: ENSP00000412492.2:p.Met858Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2572A>G
  hgvsp: ENSP00000428215.1:p.Met858Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.595A>G
  hgvsp: ENSP00000430255.1:p.Met199Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2557A>G
  hgvsp: ENSP00000195649.6:p.Met853Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2282A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2572A>G
  hgvsp: ENSP00000400459.2:p.Met858Val
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2482A>G
  hgvsp: ENSP00000428511.1:p.Met828Val
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18507
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met858Val
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/6-84269884-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269884
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269884
    reference: chr 6
allele count: 6
allele frequency: 4.978757302177376e-5
allele num: 120512
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2480T>G
  hgvsp: ENSP00000428511.1:p.Val827Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.593T>G
  hgvsp: ENSP00000430255.1:p.Val198Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1649T>G
  hgvsp: ENSP00000428026.1:p.Val550Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2570T>G
  hgvsp: ENSP00000400459.2:p.Val857Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2570T>G
  hgvsp: ENSP00000358708.2:p.Val857Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2570T>G
  hgvsp: ENSP00000412492.2:p.Val857Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2661T>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2555T>G
  hgvsp: ENSP00000195649.6:p.Val852Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2555T>G
  hgvsp: ENSP00000429776.1:p.Val852Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2570T>G
  hgvsp: ENSP00000428215.1:p.Val857Gly
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2280T>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1649T>G
  hgvsp: ENSP00000413277.1:p.Val550Gly
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val857Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

6-84269886-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269886
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269886
    reference: chr 6
allele count: 1
allele frequency: 8.299443937256203e-6
allele num: 120490
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.591G>A
  hgvsp: ENST00000523448.1:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2478G>A
  hgvsp: ENST00000520302.1:c.2478G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1647G>A
  hgvsp: ENST00000520213.1:c.1647G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2568G>A
  hgvsp: ENST00000439399.2:c.2568G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2553G>A
  hgvsp: ENST00000521485.1:c.2553G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2568G>A
  hgvsp: ENST00000369694.2:c.2568G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2278G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1647G>A
  hgvsp: ENST00000437520.1:c.1647G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2568G>A
  hgvsp: ENST00000521743.1:c.2568G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2553G>A
  hgvsp: ENST00000195649.6:c.2553G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2659G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2568G>A
  hgvsp: ENST00000428679.2:c.2568G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro856Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

6-84269887-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269887
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269887
    reference: chr 6
allele count: 1
allele frequency: 8.300546175938376e-6
allele num: 120474
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2567C>T
  hgvsp: ENSP00000358708.2:p.Pro856Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2658C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2567C>T
  hgvsp: ENSP00000412492.2:p.Pro856Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2552C>T
  hgvsp: ENSP00000195649.6:p.Pro851Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1646C>T
  hgvsp: ENSP00000413277.1:p.Pro549Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1646C>T
  hgvsp: ENSP00000428026.1:p.Pro549Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2277C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2552C>T
  hgvsp: ENSP00000429776.1:p.Pro851Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2567C>T
  hgvsp: ENSP00000428215.1:p.Pro856Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.590C>T
  hgvsp: ENSP00000430255.1:p.Pro197Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2567C>T
  hgvsp: ENSP00000400459.2:p.Pro856Leu
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2477C>T
  hgvsp: ENSP00000428511.1:p.Pro826Leu
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro856Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

6-84269901-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269901
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269901
    reference: chr 6
allele count: 1
allele frequency: 8.309788931361144e-6
allele num: 120340
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2553G>A
  hgvsp: ENSP00000400459.2:p.Met851Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.576G>A
  hgvsp: ENSP00000430255.1:p.Met192Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1632G>A
  hgvsp: ENSP00000413277.1:p.Met544Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2553G>A
  hgvsp: ENSP00000428215.1:p.Met851Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1632G>A
  hgvsp: ENSP00000428026.1:p.Met544Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2538G>A
  hgvsp: ENSP00000429776.1:p.Met846Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2553G>A
  hgvsp: ENSP00000412492.2:p.Met851Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2263G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2538G>A
  hgvsp: ENSP00000195649.6:p.Met846Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2553G>A
  hgvsp: ENSP00000358708.2:p.Met851Ile
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2644G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2463G>A
  hgvsp: ENSP00000428511.1:p.Met821Ile
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met851Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

6-84269927-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269927
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269927
    reference: chr 6
allele count: 1
allele frequency: 8.360784576024614e-6
allele num: 119606
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2618C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1606C>A
  hgvsp: ENSP00000428026.1:p.Pro536Thr
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2437C>A
  hgvsp: ENSP00000428511.1:p.Pro813Thr
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.550C>A
  hgvsp: ENSP00000430255.1:p.Pro184Thr
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2527C>A
  hgvsp: ENSP00000412492.2:p.Pro843Thr
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2527C>A
  hgvsp: ENSP00000428215.1:p.Pro843Thr
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2237C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2527C>A
  hgvsp: ENSP00000358708.2:p.Pro843Thr
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2527C>A
  hgvsp: ENSP00000400459.2:p.Pro843Thr
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2512C>A
  hgvsp: ENSP00000195649.6:p.Pro838Thr
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2512C>A
  hgvsp: ENSP00000429776.1:p.Pro838Thr
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1606C>A
  hgvsp: ENSP00000413277.1:p.Pro536Thr
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17669
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro843Thr
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

6-84269943-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269943
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269943
    reference: chr 6
allele count: 1
allele frequency: 8.410428931875526e-6
allele num: 118900
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2527-16C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2527-16C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.550-16C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2527-16C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2437-16C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1606-16C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2527-16C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2512-16C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1606-16C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2237-16C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2512-16C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2618-16C>T
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13641
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ

6-84269950-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269950
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269950
    reference: chr 6
allele count: 1
allele frequency: 8.433694295449179e-6
allele num: 118572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2527-23C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1606-23C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2237-23C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2512-23C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1606-23C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2527-23C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2527-23C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2527-23C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2437-23C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.550-23C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2618-23C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2512-23C>A
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15985
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

6-84269965-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269965
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269965
    reference: chr 6
allele count: 1
allele frequency: 8.505715841045183e-6
allele num: 117568
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2512-38A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2527-38A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2618-38A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2237-38A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2527-38A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2527-38A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2527-38A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.550-38A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2437-38A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1606-38A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1606-38A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2512-38A>G
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum

6-84269967-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84269967
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84269967
    reference: chr 6
allele count: 1
allele frequency: 8.516291665956975e-6
allele num: 117422
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.550-40C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2237-40C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1606-40C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2527-40C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1606-40C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2512-40C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2527-40C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2618-40C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2512-40C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2527-40C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2527-40C>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2437-40C>A
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10705
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

6-84270538-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84270538
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84270538
    reference: chr 6
allele count: 1
allele frequency: 9.409639234431752e-6
allele num: 106274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2526+45T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.549+45T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2526+45T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2436+45T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2511+45T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2511+45T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1605+45T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2526+45T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1605+45T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2526+45T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2236+45T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2617+45T>C
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

6-84270540-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84270540
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84270540
    reference: chr 6
allele count: 46
allele frequency: 4.324934185784129e-4
allele num: 106360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2526+43A>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2511+43A>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2526+43A>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1605+43A>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2236+43A>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1605+43A>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2436+43A>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2526+43A>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2617+43A>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2511+43A>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.549+43A>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2526+43A>C
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10649
  bin: 1.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14526
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16306
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6614
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP

6-84270570-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84270570
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84270570
    reference: chr 6
allele count: 1
allele frequency: 8.670169415110372e-6
allele num: 115338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2526+13G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.549+13G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2526+13G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2436+13G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2617+13G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2526+13G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2511+13G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1605+13G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2236+13G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2526+13G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2511+13G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1605+13G>A
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38199
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD

6-84270571-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84270571
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84270571
    reference: chr 6
allele count: 7
allele frequency: 6.043756799226399e-5
allele num: 115822
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.549+12C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2526+12C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1605+12C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2511+12C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2617+12C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2526+12C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2526+12C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2236+12C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2511+12C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2526+12C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2436+12C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1605+12C>T
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38545
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10831
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

6-84270576-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84270576
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84270576
    reference: chr 6
allele count: 1
allele frequency: 8.56091088091773e-6
allele num: 116810
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2511+7G>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1605+7G>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2526+7G>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2436+7G>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2526+7G>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1605+7G>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2526+7G>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2617+7G>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2511+7G>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2526+7G>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2236+7G>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.549+7G>C
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39075
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2526+7G>C
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-84270592-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84270592
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84270592
    reference: chr 6
allele count: 2
allele frequency: 1.686369078736572e-5
allele num: 118598
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2517A>G
  hgvsp: ENST00000369694.2:c.2517A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2227A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.540A>G
  hgvsp: ENST00000523448.1:c.540A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2427A>G
  hgvsp: ENST00000520302.1:c.2427A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2517A>G
  hgvsp: ENST00000521743.1:c.2517A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1596A>G
  hgvsp: ENST00000520213.1:c.1596A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1596A>G
  hgvsp: ENST00000437520.1:c.1596A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2502A>G
  hgvsp: ENST00000195649.6:c.2502A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2517A>G
  hgvsp: ENST00000439399.2:c.2517A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2608A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2502A>G
  hgvsp: ENST00000521485.1:c.2502A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2517A>G
  hgvsp: ENST00000428679.2:c.2517A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39675
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly839Gly
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

6-84270601-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84270601
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84270601
    reference: chr 6
allele count: 600
allele frequency: 5.040661334767121e-3
allele num: 119032
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2508T>C
  hgvsp: ENST00000428679.2:c.2508T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2418T>C
  hgvsp: ENST00000520302.1:c.2418T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2218T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1587T>C
  hgvsp: ENST00000437520.1:c.1587T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1587T>C
  hgvsp: ENST00000520213.1:c.1587T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2493T>C
  hgvsp: ENST00000521485.1:c.2493T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2508T>C
  hgvsp: ENST00000369694.2:c.2508T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2508T>C
  hgvsp: ENST00000521743.1:c.2508T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2599T>C
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.531T>C
  hgvsp: ENST00000523448.1:c.531T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2493T>C
  hgvsp: ENST00000195649.6:c.2493T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2508T>C
  hgvsp: ENST00000439399.2:c.2508T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 3.75e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 3.25e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 39144
  bin: 2.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro836Pro
num of homozygotes: 5
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-84270603-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84270603
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84270603
    reference: chr 6
allele count: 2
allele frequency: 1.679120141046092e-5
allele num: 119110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1585C>T
  hgvsp: ENSP00000413277.1:p.Pro529Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.529C>T
  hgvsp: ENSP00000430255.1:p.Pro177Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2491C>T
  hgvsp: ENSP00000429776.1:p.Pro831Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2416C>T
  hgvsp: ENSP00000428511.1:p.Pro806Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2506C>T
  hgvsp: ENSP00000358708.2:p.Pro836Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1585C>T
  hgvsp: ENSP00000428026.1:p.Pro529Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2506C>T
  hgvsp: ENSP00000400459.2:p.Pro836Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2491C>T
  hgvsp: ENSP00000195649.6:p.Pro831Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2597C>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2506C>T
  hgvsp: ENSP00000428215.1:p.Pro836Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2506C>T
  hgvsp: ENSP00000412492.2:p.Pro836Ser
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2216C>T
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro836Ser
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

6-84270604-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84270604
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84270604
    reference: chr 6
allele count: 2
allele frequency: 1.678866429386878e-5
allele num: 119128
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1584A>G
  hgvsp: ENST00000437520.1:c.1584A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2215A>G
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2505A>G
  hgvsp: ENST00000521743.1:c.2505A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2490A>G
  hgvsp: ENST00000521485.1:c.2490A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2505A>G
  hgvsp: ENST00000439399.2:c.2505A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1584A>G
  hgvsp: ENST00000520213.1:c.1584A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2505A>G
  hgvsp: ENST00000428679.2:c.2505A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2415A>G
  hgvsp: ENST00000520302.1:c.2415A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2490A>G
  hgvsp: ENST00000195649.6:c.2490A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.528A>G
  hgvsp: ENST00000523448.1:c.528A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2505A>G
  hgvsp: ENST00000369694.2:c.2505A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2596A>G
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln835Gln
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

6-84270607-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84270607
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84270607
    reference: chr 6
allele count: 1
allele frequency: 8.386588168201411e-6
allele num: 119238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2502A>T
  hgvsp: ENST00000521743.1:c.2502A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2502A>T
  hgvsp: ENST00000439399.2:c.2502A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2502A>T
  hgvsp: ENST00000369694.2:c.2502A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1581A>T
  hgvsp: ENST00000520213.1:c.1581A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.525A>T
  hgvsp: ENST00000523448.1:c.525A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2502A>T
  hgvsp: ENST00000428679.2:c.2502A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1581A>T
  hgvsp: ENST00000437520.1:c.1581A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2487A>T
  hgvsp: ENST00000195649.6:c.2487A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2212A>T
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2487A>T
  hgvsp: ENST00000521485.1:c.2487A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2412A>T
  hgvsp: ENST00000520302.1:c.2412A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2593A>T
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly834Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD

6-84270613-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84270613
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 84270613
    reference: chr 6
allele count: 344
allele frequency: 2.883632035140074e-3
allele num: 119294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428215
  ensembl transcript: ENST00000521743
  gene symbol: SNAP91
  hgvsc: ENST00000521743.1:c.2496G>A
  hgvsp: ENST00000521743.1:c.2496G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428026
  ensembl transcript: ENST00000520213
  gene symbol: SNAP91
  hgvsc: ENST00000520213.1:c.1575G>A
  hgvsp: ENST00000520213.1:c.1575G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000358708
  ensembl transcript: ENST00000369694
  gene symbol: SNAP91
  hgvsc: ENST00000369694.2:c.2496G>A
  hgvsp: ENST00000369694.2:c.2496G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000430255
  ensembl transcript: ENST00000523448
  gene symbol: SNAP91
  hgvsc: ENST00000523448.1:c.519G>A
  hgvsp: ENST00000523448.1:c.519G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000400459
  ensembl transcript: ENST00000439399
  gene symbol: SNAP91
  hgvsc: ENST00000439399.2:c.2496G>A
  hgvsp: ENST00000439399.2:c.2496G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429937
  ensembl transcript: ENST00000518312
  gene symbol: SNAP91
  hgvsc: ENST00000518312.1:c.*2587G>A
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428511
  ensembl transcript: ENST00000520302
  gene symbol: SNAP91
  hgvsc: ENST00000520302.1:c.2406G>A
  hgvsp: ENST00000520302.1:c.2406G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000413277
  ensembl transcript: ENST00000437520
  gene symbol: SNAP91
  hgvsc: ENST00000437520.1:c.1575G>A
  hgvsp: ENST00000437520.1:c.1575G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000195649
  ensembl transcript: ENST00000195649
  gene symbol: SNAP91
  hgvsc: ENST00000195649.6:c.2481G>A
  hgvsp: ENST00000195649.6:c.2481G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000429776
  ensembl transcript: ENST00000521485
  gene symbol: SNAP91
  hgvsc: ENST00000521485.1:c.2481G>A
  hgvsp: ENST00000521485.1:c.2481G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000412492
  ensembl transcript: ENST00000428679
  gene symbol: SNAP91
  hgvsc: ENST00000428679.2:c.2496G>A
  hgvsp: ENST00000428679.2:c.2496G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000065609
  ensembl protein: ENSP00000428127
  ensembl transcript: ENST00000521616
  gene symbol: SNAP91
  hgvsc: ENST00000521616.1:c.*2206G>A
  variant of: http://identifiers.org/hgnc/14986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3263
  bin: 3.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 3.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 13125
  bin: 2.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 4.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: p.Ser832Ser
num of homozygotes: 1
reference allele: C

GenotypeDepth
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7074
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3625
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 406
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26221
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2173
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3825
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 340
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9180
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.301744337412132e-4
allele num: 7682
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2234
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.528e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

DP
type: SiteQuality
SIO_000300: 4.85078e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.784e0

MQ
type: SiteQuality
SIO_000300: 5.923e1

QD
type: SiteQuality
SIO_000300: 1.409e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.634e0

FS
type: SiteQuality
SIO_000300: 5.016e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.56e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

GenotypeDepth
all individuals: 192
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4453
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3443
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27965
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1597
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5596
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 257
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 373
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2833
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.084598698481562e-4
allele num: 9220
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7744
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.97e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.99e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.139e0

DP
type: SiteQuality
SIO_000300: 4.93446e5

QD
type: SiteQuality
SIO_000300: 9.470000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.89e-1

MQ
type: SiteQuality
SIO_000300: 5.816e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 1195
bin: 1.75e1
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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
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 6.25e1
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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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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

South 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: 1610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2256
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.529051987767584e-3
allele num: 654
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.31848e5

FS
type: SiteQuality
SIO_000300: 3.979e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.473e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.12e0

MQRankSum
type: SiteQuality
SIO_000300: 1.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-2

QD
type: SiteQuality
SIO_000300: 9.49e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.761e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.273560876209883e-4
allele num: 7852
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9436
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.098e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.31e0

FS
type: SiteQuality
SIO_000300: 3.174e0

DP
type: SiteQuality
SIO_000300: 5.40473e5

VQSLOD
type: SiteQuality
SIO_000300: -2.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.14e-2

MQ
type: SiteQuality
SIO_000300: 5.917e1

MQRankSum
type: SiteQuality
SIO_000300: 3.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.539e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

GenotypeDepth
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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
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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: 34
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variant carriers: 0

GenotypeQuality
all individuals: 14171
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9958
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1660
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.264862130027827e-4
allele num: 7906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 714
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.5e0

DP
type: SiteQuality
SIO_000300: 5.84699e5

MQ
type: SiteQuality
SIO_000300: 5.83e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e0

BaseQRankSum
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SIO_000300: -1.373e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.053e0

QD
type: SiteQuality
SIO_000300: 1.266e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.99e0

GenotypeDepth
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variant carriers: 8

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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variant carriers: 15

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 38
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GenotypeQuality
all individuals: 1405
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GenotypeQuality
all individuals: 6616
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

African
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allele count: 14
allele frequency: 5.897219882055603e-3
allele num: 2374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1702
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7940
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.48e-1

DP
type: SiteQuality
SIO_000300: 6.07934e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

FS
type: SiteQuality
SIO_000300: 1.768e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

QD
type: SiteQuality
SIO_000300: 1.221e1

GenotypeDepth
all individuals: 192
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 265
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GenotypeQuality
all individuals: 168
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10868
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.255650426921145e-4
allele num: 7964
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 498
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2456
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1738
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.338e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.297e0

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-1

DP
type: SiteQuality
SIO_000300: 6.37105e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.5e-1

MQ
type: SiteQuality
SIO_000300: 5.697e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.05e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.78e-1

QD
type: SiteQuality
SIO_000300: 1.499e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 5.696614583333334e-4
allele num: 12288
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8038
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 994
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2700
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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DP
type: SiteQuality
SIO_000300: 6.85538e5

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.361e0

ClippingRankSum
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SIO_000300: -3.58e-1

VQSLOD
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MQ
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SIO_000300: 5.833e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.04e-2

QD
type: SiteQuality
SIO_000300: 1.082e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
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SIO_000300: 3.22e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2710
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12486
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1018
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1848
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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QD
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VQSLOD
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SIO_000300: -1.105e0

MQRankSum
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SIO_000300: -3.22e-1

ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1916
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.540357362908195e-4
allele num: 12984
num of homozygotes: 0

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

South Asian
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ReadPosRankSum
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MQRankSum
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QD
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FS
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BaseQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 7.24952878062926e-5
allele num: 13794
num of homozygotes: 0

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

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele frequency: 7.057163020465773e-5
allele num: 14170
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 8.622041072268381e-4
allele num: 12758
num of homozygotes: 0

South Asian
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Latino
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allele frequency: 0.0e0
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Other
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European (Finnish)
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allele frequency: 5.369928400954654e-3
allele num: 1676
num of homozygotes: 0

African
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ReadPosRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2822
num of homozygotes: 0

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

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

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

Latino
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Other
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African
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European (Non-Finnish)
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allele frequency: 9.493070058857034e-5
allele num: 10534
num of homozygotes: 0

East Asian
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InbreedingCoeff
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MQ
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MQRankSum
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ClippingRankSum
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VQSLOD
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QD
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ReadPosRankSum
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BaseQRankSum
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DP
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FS
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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South Asian
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African
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European (Non-Finnish)
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Latino
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Other
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QD
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FS
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DP
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BaseQRankSum
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ClippingRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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African
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European (Non-Finnish)
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South Asian
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Latino
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European (Finnish)
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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VQSLOD
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QD
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MQ
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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African
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European (Non-Finnish)
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East Asian
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Latino
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European (Finnish)
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VQSLOD
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MQ
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ReadPosRankSum
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FS
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QD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 66244
num of homozygotes: 0

Latino
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European (Finnish)
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South Asian
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Other
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African
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East Asian
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QD
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FS
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ClippingRankSum
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DP
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BaseQRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Non-Finnish)
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Other
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European (Finnish)
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East Asian
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Latino
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DP
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MQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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ClippingRankSum
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ReadPosRankSum
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FS
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MQ
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Finnish)
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European (Non-Finnish)
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African
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East Asian
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South Asian
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MQRankSum
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QD
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FS
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BaseQRankSum
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VQSLOD
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MQ
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DP
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ReadPosRankSum
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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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East Asian
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Latino
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South Asian
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African
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European (Non-Finnish)
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Other
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European (Finnish)
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BaseQRankSum
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SIO_000300: 3.37e0

VQSLOD
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ClippingRankSum
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SIO_000300: -9.85e-1

InbreedingCoeff
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SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.486e1

DP
type: SiteQuality
SIO_000300: 1.882351e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66394
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

African
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allele count: 2
allele frequency: 2.050861361771944e-4
allele num: 9752
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.35e-1

MQRankSum
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ClippingRankSum
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FS
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MQ
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VQSLOD
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DP
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InbreedingCoeff
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SIO_000300: 1.6e-3

QD
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SIO_000300: 1.218e1

BaseQRankSum
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SIO_000300: -2.05e0

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505026789476853e-5
allele num: 66444
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.41e-1

QD
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SIO_000300: 1.368e1

FS
type: SiteQuality
SIO_000300: 3.827e0

InbreedingCoeff
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SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.703e1

BaseQRankSum
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SIO_000300: 2.36e0

DP
type: SiteQuality
SIO_000300: 1.896663e6

VQSLOD
type: SiteQuality
SIO_000300: -3.271e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.66e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 102
bin: 3.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9778
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503578516870151e-5
allele num: 66508
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -1.481e0

MQRankSum
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SIO_000300: -1.029e0

QD
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SIO_000300: 5.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.79e-1

InbreedingCoeff
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SIO_000300: 1.0e-4

ReadPosRankSum
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SIO_000300: 1.13e0

VQSLOD
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SIO_000300: -1.891e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.901041e6

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
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: 11482
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502855425308085e-5
allele num: 66540
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.81e0

InbreedingCoeff
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QD
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VQSLOD
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FS
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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SIO_000300: 5.934e1

DP
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SIO_000300: 1.902476e6

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 33
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variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.688097306689835e-5
allele num: 11510
num of homozygotes: 0

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

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

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

Other
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allele frequency: 0.0e0
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African
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allele count: 1
allele frequency: 1.021659174499387e-4
allele num: 9788
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.002462018855461e-5
allele num: 66612
num of homozygotes: 0

BaseQRankSum
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ReadPosRankSum
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FS
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MQ
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MQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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VQSLOD
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QD
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GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 3.475238922675934e-4
allele num: 11510
num of homozygotes: 0

East Asian
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African
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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allele frequency: 2.423948612289419e-4
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.002462018855461e-5
allele num: 66612
num of homozygotes: 0

Other
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ClippingRankSum
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MQ
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ReadPosRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513317191283293e-4
allele num: 6608
num of homozygotes: 0

Other
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African
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allele num: 9790
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 1
allele frequency: 8.685079034219212e-5
allele num: 11514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66622
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South Asian
type: Population
allele count: 3
allele frequency: 1.817961459217065e-4
allele num: 16502
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MQ
type: SiteQuality
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ClippingRankSum
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VQSLOD
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
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SIO_000300: 1.905684e6

BaseQRankSum
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SIO_000300: 2.29e0

InbreedingCoeff
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SIO_000300: 7.0e-4

QD
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 2.423654871546292e-4
allele num: 16504
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

ClippingRankSum
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SIO_000300: -3.33e-1

InbreedingCoeff
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BaseQRankSum
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FS
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VQSLOD
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QD
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SIO_000300: 1.098e1

MQRankSum
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DP
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SIO_000300: 1.905941e6

MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 7.98e-1

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

African
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allele count: 2
allele frequency: 2.043318348998774e-4
allele num: 9788
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 9.004141905276428e-5
allele num: 66636
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 8.0e-4

DP
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SIO_000300: 1.906565e6

ReadPosRankSum
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SIO_000300: 9.65e-1

VQSLOD
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ClippingRankSum
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SIO_000300: -4.31e-1

MQ
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SIO_000300: 5.964e1

MQRankSum
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BaseQRankSum
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SIO_000300: -8.2e-1

QD
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SIO_000300: 1.202e1

FS
type: SiteQuality
SIO_000300: 5.89e-1

GenotypeDepth
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66634
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

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

InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQ
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FS
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MQRankSum
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VQSLOD
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DP
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BaseQRankSum
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QD
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GenotypeDepth
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variant carriers: 0

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

East Asian
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South Asian
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African
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Latino
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allele num: 11526
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European (Non-Finnish)
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allele count: 0
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num of homozygotes: 0

Other
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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MQ
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FS
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BaseQRankSum
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QD
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MQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

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

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

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.977e1

DP
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SIO_000300: 1.90648e6

FS
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SIO_000300: 5.967e0

ReadPosRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQRankSum
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SIO_000300: -6.37e-1

QD
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InbreedingCoeff
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SIO_000300: 3.0e-4

GenotypeDepth
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variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 6.070908207867897e-5
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num of homozygotes: 0

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

Latino
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MQ
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ReadPosRankSum
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FS
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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ClippingRankSum
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QD
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SIO_000300: 1.272e1

InbreedingCoeff
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SIO_000300: 1.0e-3

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

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

African
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allele count: 4
allele frequency: 4.085801838610827e-4
allele num: 9790
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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South Asian
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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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ClippingRankSum
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MQ
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SIO_000300: 6.0e1

MQRankSum
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FS
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DP
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InbreedingCoeff
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ReadPosRankSum
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SIO_000300: 7.18e-1

VQSLOD
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QD
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SIO_000300: 9.880000000000001e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.075334143377886e-5
allele num: 16460
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
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MQRankSum
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FS
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BaseQRankSum
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MQ
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ReadPosRankSum
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DP
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VQSLOD
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InbreedingCoeff
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SIO_000300: 1.2e-3

QD
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 6
allele frequency: 9.007115621340859e-5
allele num: 66614
num of homozygotes: 0

African
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European (Finnish)
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Latino
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South Asian
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East Asian
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Other
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MQRankSum
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QD
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BaseQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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European (Finnish)
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East Asian
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Latino
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Other
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MQ
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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FS
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DP
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QD
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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East Asian
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FS
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BaseQRankSum
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MQ
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DP
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 1.502584445245823e-5
allele num: 66552
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 9752
num of homozygotes: 0

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

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

Other
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European (Finnish)
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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MQ
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QD
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FS
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BaseQRankSum
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MQRankSum
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DP
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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Other
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European (Non-Finnish)
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African
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European (Finnish)
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East Asian
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InbreedingCoeff
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MQRankSum
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FS
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VQSLOD
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DP
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ClippingRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2614
bin: 9.75e1
variant carriers: 43

GenotypeQuality
all individuals: 229
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3333
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 9.25e1
variant carriers: 2

Latino
type: Population
allele count: 5
allele frequency: 5.149330587023687e-4
allele num: 9710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 39
allele frequency: 6.583167347489956e-4
allele num: 59242
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.32396002788752e-4
allele num: 8606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14430
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e-1

QD
type: SiteQuality
SIO_000300: 1.462e1

DP
type: SiteQuality
SIO_000300: 1.191177e6

GenotypeDepth
all individuals: 2193
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1019
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43491
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
all individuals: 912
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2582
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 994
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15418
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8282
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9312
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10918
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.559527151367705e-5
allele num: 64122
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6440
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.49e-1

FS
type: SiteQuality
SIO_000300: 7.031e0

DP
type: SiteQuality
SIO_000300: 1.463003e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e0

MQRankSum
type: SiteQuality
SIO_000300: -4.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.736e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.146e1

GenotypeDepth
all individuals: 502
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1012
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44336
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2592
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 7.5e0
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GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2590
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 463
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1029
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.444960041247745e-5
allele num: 15516
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9348
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64358
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 7.218479307025986e-4
allele num: 8312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

DP
type: SiteQuality
SIO_000300: 1.471757e6

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-1

QD
type: SiteQuality
SIO_000300: 1.247e1

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.37e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.418e0

GenotypeDepth
all individuals: 108
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 99
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4722
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variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1058
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2582
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 335
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45278
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.542590935735662e-5
allele num: 64826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15676
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11106
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.315e0

VQSLOD
type: SiteQuality
SIO_000300: -1.691e-1

DP
type: SiteQuality
SIO_000300: 1.485819e6

QD
type: SiteQuality
SIO_000300: 1.293e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.883e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

GenotypeDepth
all individuals: 108
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 102
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 115
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
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variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 9.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 5001
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variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 46728
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1087
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1259
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2584
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 248
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1094
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.042843232716651e-5
allele num: 65728
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16008
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.96e-1

QD
type: SiteQuality
SIO_000300: 9.93e0

DP
type: SiteQuality
SIO_000300: 1.51123e6

GenotypeDepth
all individuals: 114
bin: 8.25e1
variant carriers: 6

GenotypeDepth
all individuals: 487
bin: 4.25e1
variant carriers: 83

GenotypeDepth
all individuals: 133
bin: 6.75e1
variant carriers: 4

GenotypeDepth
all individuals: 12626
bin: 2.75e1
variant carriers: 66

GenotypeQuality
all individuals: 1098
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4982
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 153
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1073
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 590
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 56
bin: 7.5e0
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GenotypeQuality
all individuals: 246
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3132
bin: 9.75e1
variant carriers: 589

GenotypeQuality
all individuals: 256
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46521
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 301
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 155
bin: 4.75e1
variant carriers: 1

African
type: Population
allele count: 6
allele frequency: 6.208609271523179e-4
allele num: 9664
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

Latino
type: Population
allele count: 33
allele frequency: 2.905441098784997e-3
allele num: 11358
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 40
allele frequency: 6.086427267194157e-3
allele num: 6572
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 7.46175848775028e-4
allele num: 16082
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 504
allele frequency: 7.642616686379765e-3
allele num: 65946
num of homozygotes: 5

Other
type: Population
allele count: 5
allele frequency: 5.773672055427252e-3
allele num: 866
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.3e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

DP
type: SiteQuality
SIO_000300: 1.530258e6

QD
type: SiteQuality
SIO_000300: 1.088e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.304e0

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-2

GenotypeDepth
all individuals: 183
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 114
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variant carriers: 0

GenotypeDepth
all individuals: 3187
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 101
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GenotypeQuality
all individuals: 153
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GenotypeQuality
all individuals: 55
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GenotypeQuality
all individuals: 47078
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GenotypeQuality
all individuals: 1101
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variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 4.75e1
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GenotypeQuality
all individuals: 244
bin: 2.75e1
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GenotypeQuality
all individuals: 93
bin: 4.25e1
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GenotypeQuality
all individuals: 1129
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variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 5.25e1
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 1041
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GenotypeQuality
all individuals: 253
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GenotypeQuality
all individuals: 2564
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5067
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GenotypeQuality
all individuals: 602
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GenotypeQuality
all individuals: 220
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GenotypeQuality
all individuals: 307
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GenotypeQuality
all individuals: 117
bin: 5.75e1
variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.242390359050814e-4
allele num: 16098
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65994
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.550000000000001e0

FS
type: SiteQuality
SIO_000300: 8.762e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.345e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: -3.805e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

DP
type: SiteQuality
SIO_000300: 1.522992e6

GenotypeDepth
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3187
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variant carriers: 1

GenotypeDepth
all individuals: 101
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GenotypeDepth
all individuals: 170
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GenotypeQuality
all individuals: 215
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 240
bin: 2.75e1
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GenotypeQuality
all individuals: 243
bin: 5.25e1
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GenotypeQuality
all individuals: 54
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GenotypeQuality
all individuals: 1106
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GenotypeQuality
all individuals: 146
bin: 3.75e1
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GenotypeQuality
all individuals: 306
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variant carriers: 0

GenotypeQuality
all individuals: 1130
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 249
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5081
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2564
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 152
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47022
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1042
bin: 2.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16096
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

QD
type: SiteQuality
SIO_000300: 1.479e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.86e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.04e-1

FS
type: SiteQuality
SIO_000300: 6.54e-1

DP
type: SiteQuality
SIO_000300: 1.523121e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

GenotypeDepth
all individuals: 13019
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 182
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 99
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2564
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 152
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47035
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 92
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5089
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 239
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1001
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16120
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.033484911120298e-4
allele num: 9676
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66060
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.24e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.496e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.64e-1

DP
type: SiteQuality
SIO_000300: 1.524583e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.53e0

MQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.192e1

GenotypeDepth
all individuals: 185
bin: 6.25e1
variant carriers: 16

GenotypeDepth
all individuals: 452
bin: 4.25e1
variant carriers: 46

GenotypeDepth
all individuals: 38695
bin: 2.25e1
variant carriers: 24

GenotypeDepth
all individuals: 420
bin: 1.75e1
variant carriers: 9

GenotypeQuality
all individuals: 575
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46603
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5047
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1004
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2863
bin: 9.75e1
variant carriers: 341

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