12-56120899-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120899
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120899
    reference: chr 12
allele count: 2
allele frequency: 1.706572008805912e-5
allele num: 117194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.255+36G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.9+36G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.255+36G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.255+36G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.186+36G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.255+36G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.255+36G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.255+36G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449684
  ensembl transcript: ENST00000552067
  gene symbol: CD63
  hgvsc: ENST00000552067.1:c.-57G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.255+36G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.9+36G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.255+36G>A
  variant of: http://identifiers.org/hgnc/1692
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

12-56120902-A-ATG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120902
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120904
    reference: chr 12
allele count: 2
allele frequency: 1.704129104820981e-5
allele num: 117362
alternate allele: ATG
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.255+32_255+33insCA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.255+32_255+33insCA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.186+32_186+33insCA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.255+32_255+33insCA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.9+32_9+33insCA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.255+32_255+33insCA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.255+32_255+33insCA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.255+32_255+33insCA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.255+32_255+33insCA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449684
  ensembl transcript: ENST00000552067
  gene symbol: CD63
  hgvsc: ENST00000552067.1:c.-61_-60insCA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.255+32_255+33insCA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.9+32_9+33insCA
  variant of: http://identifiers.org/hgnc/1692
canonical: false
consequence: 5' UTR
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

12-56120903-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120903
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120903
    reference: chr 12
allele count: 1
allele frequency: 8.521081154776918e-6
allele num: 117356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.186+32C>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.9+32C>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449684
  ensembl transcript: ENST00000552067
  gene symbol: CD63
  hgvsc: ENST00000552067.1:c.-61C>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.255+32C>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.255+32C>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.255+32C>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.255+32C>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.255+32C>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.255+32C>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.255+32C>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.9+32C>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.255+32C>G
  variant of: http://identifiers.org/hgnc/1692
canonical: false
consequence: 5' UTR
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 10737
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

12-56120903-GACC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120903
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120900
    reference: chr 12
allele count: 2
allele frequency: 1.704216230955384e-5
allele num: 117356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.9+29_9+31delGGT
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.255+29_255+31delGGT
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.255+29_255+31delGGT
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.9+29_9+31delGGT
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.255+29_255+31delGGT
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.255+29_255+31delGGT
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.255+29_255+31delGGT
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449684
  ensembl transcript: ENST00000552067
  gene symbol: CD63
  hgvsc: ENST00000552067.1:c.-64_-62delGGT
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.255+29_255+31delGGT
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.255+29_255+31delGGT
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.186+29_186+31delGGT
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.255+29_255+31delGGT
  variant of: http://identifiers.org/hgnc/1692
canonical: false
consequence: 5' UTR
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10737
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6713
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: GACC
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/12-56120905-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120905
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120905
    reference: chr 12
allele count: 3
allele frequency: 2.557108762359359e-5
allele num: 117320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.255+30G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.9+30G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.255+30G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.255+30G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.255+30G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.255+30G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449684
  ensembl transcript: ENST00000552067
  gene symbol: CD63
  hgvsc: ENST00000552067.1:c.-63G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.255+30G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.9+30G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.255+30G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.255+30G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.186+30G>T
  variant of: http://identifiers.org/hgnc/1692
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

12-56120905-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120905
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120905
    reference: chr 12
allele count: 1
allele frequency: 8.523695874531197e-6
allele num: 117320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449684
  ensembl transcript: ENST00000552067
  gene symbol: CD63
  hgvsc: ENST00000552067.1:c.-63G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.255+30G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.9+30G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.255+30G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.186+30G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.9+30G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.255+30G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.255+30G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.255+30G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.255+30G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.255+30G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.255+30G>A
  variant of: http://identifiers.org/hgnc/1692
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

12-56120907-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120907
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120907
    reference: chr 12
allele count: 2
allele frequency: 1.702446415499072e-5
allele num: 117478
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.255+28C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.9+28C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.255+28C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.255+28C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.186+28C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.255+28C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449684
  ensembl transcript: ENST00000552067
  gene symbol: CD63
  hgvsc: ENST00000552067.1:c.-65C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.255+28C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.255+28C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.255+28C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.9+28C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.255+28C>T
  variant of: http://identifiers.org/hgnc/1692
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8415
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

12-56120908-CCCATGTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120908
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120901
    reference: chr 12
allele count: 2
allele frequency: 1.700795972515137e-5
allele num: 117592
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.255+20_255+26delAACATGG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.255+20_255+26delAACATGG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.9+20_9+26delAACATGG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.255+20_255+26delAACATGG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.255+20_255+26delAACATGG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.9+20_9+26delAACATGG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.255+20_255+26delAACATGG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449684
  ensembl transcript: ENST00000552067
  gene symbol: CD63
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.255+20_255+26delAACATGG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.255+20_255+26delAACATGG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.186+20_186+26delAACATGG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.255+20_255+26delAACATGG
  variant of: http://identifiers.org/hgnc/1692
canonical: false
consequence: 5' UTR
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: CCCATGTT
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS

12-56120911-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120911
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120912
    reference: chr 12
allele count: 2
allele frequency: 1.698398410299088e-5
allele num: 117758
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.9+23dupA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.186+23dupA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.255+23dupA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.255+23dupA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.9+23dupA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.255+23dupA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449684
  ensembl transcript: ENST00000552067
  gene symbol: CD63
  hgvsc: ENST00000552067.1:c.-70dupA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.255+23dupA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.255+23dupA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.255+23dupA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.255+23dupA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.255+23dupA
  variant of: http://identifiers.org/hgnc/1692
canonical: false
consequence: 5' UTR
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

12-56120921-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120921
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120921
    reference: chr 12
allele count: 2
allele frequency: 1.694656747275839e-5
allele num: 118018
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.255+14G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.255+14G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.255+14G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.255+14G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.9+14G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.255+14G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.9+14G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.186+14G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.255+14G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.255+14G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.255+14G>A
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3755
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4195
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

12-56120922-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120922
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120922
    reference: chr 12
allele count: 3
allele frequency: 2.539747041194697e-5
allele num: 118122
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.9+13C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.186+13C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.255+13C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.255+13C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.255+13C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.255+13C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.9+13C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.255+13C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.255+13C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.255+13C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.255+13C>T
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3755
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5302
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-56120922-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120922
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120923
    reference: chr 12
allele count: 2
allele frequency: 1.693164694129798e-5
allele num: 118122
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.255+12dupG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.255+12dupG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.255+12dupG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.255+12dupG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.255+12dupG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.255+12dupG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.255+12dupG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.186+12dupG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.255+12dupG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.9+12dupG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.9+12dupG
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3755
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3533
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

12-56120922-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120922
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120921
    reference: chr 12
allele count: 3
allele frequency: 2.539747041194697e-5
allele num: 118122
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.255+12delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.255+12delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.255+12delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.255+12delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.255+12delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.9+12delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.186+12delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.255+12delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.255+12delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.255+12delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.9+12delG
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3755
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12385
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: GC
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

12-56120937-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120937
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120937
    reference: chr 12
allele count: 2
allele frequency: 1.674368762976358e-5
allele num: 119448
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.253A>T
  hgvsp: ENSP00000449337.1:p.Thr85Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.253A>T
  hgvsp: ENSP00000393502.2:p.Thr85Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.253A>T
  hgvsp: ENSP00000449435.1:p.Thr85Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.253A>T
  hgvsp: ENSP00000449281.1:p.Thr85Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.253A>T
  hgvsp: ENSP00000447730.1:p.Thr85Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.253A>T
  hgvsp: ENSP00000257857.4:p.Thr85Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.253A>T
  hgvsp: ENSP00000446752.1:p.Thr85Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.7A>T
  hgvsp: ENSP00000448091.1:p.Thr3Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.253A>T
  hgvsp: ENSP00000450191.1:p.Thr85Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.7A>T
  hgvsp: ENSP00000447356.1:p.Thr3Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.184A>T
  hgvsp: ENSP00000446807.1:p.Thr62Ser
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6710
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr85Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

12-56120938-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120938
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120938
    reference: chr 12
allele count: 1
allele frequency: 8.367080558251614e-6
allele num: 119516
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.252C>A
  hgvsp: ENST00000420846.3:c.252C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.252C>A
  hgvsp: ENST00000552164.1:c.252C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.252C>A
  hgvsp: ENST00000257857.4:c.252C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.183C>A
  hgvsp: ENST00000552754.1:c.183C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.252C>A
  hgvsp: ENST00000550050.1:c.252C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.252C>A
  hgvsp: ENST00000552692.1:c.252C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.252C>A
  hgvsp: ENST00000551173.1:c.252C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.252C>A
  hgvsp: ENST00000546457.1:c.252C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.252C>A
  hgvsp: ENST00000549117.1:c.252C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.6C>A
  hgvsp: ENST00000546939.1:c.6C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.6C>A
  hgvsp: ENST00000550776.1:c.6C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6708
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10412
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile84Ile
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD

12-56120950-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120950
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120950
    reference: chr 12
allele count: 1
allele frequency: 8.315455104857889e-6
allele num: 120258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.240T>C
  hgvsp: ENST00000552692.1:c.240T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.240T>C
  hgvsp: ENST00000420846.3:c.240T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-7T>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.240T>C
  hgvsp: ENST00000550050.1:c.240T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.240T>C
  hgvsp: ENST00000549117.1:c.240T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-7T>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.240T>C
  hgvsp: ENST00000552164.1:c.240T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.240T>C
  hgvsp: ENST00000257857.4:c.240T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.240T>C
  hgvsp: ENST00000551173.1:c.240T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.240T>C
  hgvsp: ENST00000546457.1:c.240T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.171T>C
  hgvsp: ENST00000552754.1:c.171T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6711
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10842
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr80Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-56120951-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120951
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120951
    reference: chr 12
allele count: 4
allele frequency: 3.325352487363661e-5
allele num: 120288
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.239A>G
  hgvsp: ENSP00000446752.1:p.Tyr80Cys
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.239A>G
  hgvsp: ENSP00000450191.1:p.Tyr80Cys
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.239A>G
  hgvsp: ENSP00000449435.1:p.Tyr80Cys
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-8A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.239A>G
  hgvsp: ENSP00000393502.2:p.Tyr80Cys
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.239A>G
  hgvsp: ENSP00000449281.1:p.Tyr80Cys
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.239A>G
  hgvsp: ENSP00000257857.4:p.Tyr80Cys
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.239A>G
  hgvsp: ENSP00000447730.1:p.Tyr80Cys
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.170A>G
  hgvsp: ENSP00000446807.1:p.Tyr57Cys
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.239A>G
  hgvsp: ENSP00000449337.1:p.Tyr80Cys
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-8A>G
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10842
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr80Cys
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

12-56120953-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120953
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120953
    reference: chr 12
allele count: 1
allele frequency: 8.30813199960121e-6
allele num: 120364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.237C>T
  hgvsp: ENST00000546457.1:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.237C>T
  hgvsp: ENST00000257857.4:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.237C>T
  hgvsp: ENST00000551173.1:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.168C>T
  hgvsp: ENST00000552754.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.237C>T
  hgvsp: ENST00000552692.1:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.237C>T
  hgvsp: ENST00000550050.1:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.237C>T
  hgvsp: ENST00000549117.1:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.237C>T
  hgvsp: ENST00000420846.3:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-10C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-10C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.237C>T
  hgvsp: ENST00000552164.1:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5106
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10838
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn79Asn
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

12-56120956-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120956
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120956
    reference: chr 12
allele count: 1
allele frequency: 8.300408380092301e-6
allele num: 120476
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.165G>C
  hgvsp: ENSP00000446807.1:p.Glu55Asp
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.234G>C
  hgvsp: ENSP00000450191.1:p.Glu78Asp
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.234G>C
  hgvsp: ENSP00000393502.2:p.Glu78Asp
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.234G>C
  hgvsp: ENSP00000446752.1:p.Glu78Asp
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.234G>C
  hgvsp: ENSP00000449337.1:p.Glu78Asp
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.234G>C
  hgvsp: ENSP00000449281.1:p.Glu78Asp
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.234G>C
  hgvsp: ENSP00000449435.1:p.Glu78Asp
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-13G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.234G>C
  hgvsp: ENSP00000257857.4:p.Glu78Asp
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.234G>C
  hgvsp: ENSP00000447730.1:p.Glu78Asp
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-13G>C
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10749
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu78Asp
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

12-56120971-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120971
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120971
    reference: chr 12
allele count: 2
allele frequency: 1.654314452091054e-5
allele num: 120896
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.219C>T
  hgvsp: ENST00000546457.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.219C>T
  hgvsp: ENST00000550050.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.219C>T
  hgvsp: ENST00000257857.4:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.219C>T
  hgvsp: ENST00000549117.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.219C>T
  hgvsp: ENST00000552164.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.219C>T
  hgvsp: ENST00000552692.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.219C>T
  hgvsp: ENST00000420846.3:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-28C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.219C>T
  hgvsp: ENST00000551173.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.150C>T
  hgvsp: ENST00000552754.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-28C>T
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5106
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3756
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys73Cys
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-56120977-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120977
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120977
    reference: chr 12
allele count: 1
allele frequency: 8.266375690242371e-6
allele num: 120972
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.213C>T
  hgvsp: ENST00000551173.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.213C>T
  hgvsp: ENST00000420846.3:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.213C>T
  hgvsp: ENST00000546457.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.213C>T
  hgvsp: ENST00000550050.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.144C>T
  hgvsp: ENST00000552754.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.213C>T
  hgvsp: ENST00000257857.4:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.213C>T
  hgvsp: ENST00000552692.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.213C>T
  hgvsp: ENST00000549117.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-34C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.213C>T
  hgvsp: ENST00000552164.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-34C>T
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3755
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11131
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly71Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP

12-56120982-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120982
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120982
    reference: chr 12
allele count: 2
allele frequency: 1.652592090694254e-5
allele num: 121022
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.208G>A
  hgvsp: ENSP00000449435.1:p.Val70Met
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-39G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.208G>A
  hgvsp: ENSP00000257857.4:p.Val70Met
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.208G>A
  hgvsp: ENSP00000446752.1:p.Val70Met
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.208G>A
  hgvsp: ENSP00000447730.1:p.Val70Met
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.208G>A
  hgvsp: ENSP00000450191.1:p.Val70Met
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.208G>A
  hgvsp: ENSP00000449337.1:p.Val70Met
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-39G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.208G>A
  hgvsp: ENSP00000449281.1:p.Val70Met
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.139G>A
  hgvsp: ENSP00000446807.1:p.Val47Met
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.208G>A
  hgvsp: ENSP00000393502.2:p.Val70Met
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6711
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val70Met
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

12-56120986-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120986
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120986
    reference: chr 12
allele count: 1
allele frequency: 8.261731658955718e-6
allele num: 121040
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.204T>C
  hgvsp: ENST00000420846.3:c.204T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.204T>C
  hgvsp: ENST00000551173.1:c.204T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.204T>C
  hgvsp: ENST00000552164.1:c.204T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.204T>C
  hgvsp: ENST00000552692.1:c.204T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.135T>C
  hgvsp: ENST00000552754.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.204T>C
  hgvsp: ENST00000549117.1:c.204T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.204T>C
  hgvsp: ENST00000257857.4:c.204T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.204T>C
  hgvsp: ENST00000546457.1:c.204T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.204T>C
  hgvsp: ENST00000550050.1:c.204T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-43T>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-43T>C
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6704
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala68Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

12-56120998-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56120998
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56120998
    reference: chr 12
allele count: 2
allele frequency: 1.652127940787734e-5
allele num: 121056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.192C>A
  hgvsp: ENST00000546457.1:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.192C>A
  hgvsp: ENST00000420846.3:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-55C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.192C>A
  hgvsp: ENST00000549117.1:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.192C>A
  hgvsp: ENST00000550050.1:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.123C>A
  hgvsp: ENST00000552754.1:c.123C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.192C>A
  hgvsp: ENST00000552692.1:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.192C>A
  hgvsp: ENST00000257857.4:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.192C>A
  hgvsp: ENST00000552164.1:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.192C>A
  hgvsp: ENST00000551173.1:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-55C>A
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu64Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/12-56121002-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121002
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121002
    reference: chr 12
allele count: 3
allele frequency: 2.478191911181602e-5
allele num: 121056
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.119T>G
  hgvsp: ENSP00000446807.1:p.Phe40Cys
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.188T>G
  hgvsp: ENSP00000446752.1:p.Phe63Cys
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-59T>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.188T>G
  hgvsp: ENSP00000257857.4:p.Phe63Cys
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.188T>G
  hgvsp: ENSP00000449337.1:p.Phe63Cys
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.188T>G
  hgvsp: ENSP00000449435.1:p.Phe63Cys
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-59T>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.188T>G
  hgvsp: ENSP00000393502.2:p.Phe63Cys
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.188T>G
  hgvsp: ENSP00000449281.1:p.Phe63Cys
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.188T>G
  hgvsp: ENSP00000447730.1:p.Phe63Cys
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.188T>G
  hgvsp: ENSP00000450191.1:p.Phe63Cys
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe63Cys
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

12-56121006-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121006
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121006
    reference: chr 12
allele count: 5
allele frequency: 4.130319851969337e-5
allele num: 121056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.184G>A
  hgvsp: ENSP00000449435.1:p.Val62Ile
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.184G>A
  hgvsp: ENSP00000393502.2:p.Val62Ile
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.184G>A
  hgvsp: ENSP00000446752.1:p.Val62Ile
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.184G>A
  hgvsp: ENSP00000449281.1:p.Val62Ile
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-63G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.184G>A
  hgvsp: ENSP00000449337.1:p.Val62Ile
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-63G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.184G>A
  hgvsp: ENSP00000450191.1:p.Val62Ile
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.115G>A
  hgvsp: ENSP00000446807.1:p.Val39Ile
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.184G>A
  hgvsp: ENSP00000447730.1:p.Val62Ile
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.184G>A
  hgvsp: ENSP00000257857.4:p.Val62Ile
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val62Ile
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

12-56121015-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121015
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121015
    reference: chr 12
allele count: 2
allele frequency: 1.652346331791144e-5
allele num: 121040
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.175G>A
  hgvsp: ENSP00000446752.1:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.175G>A
  hgvsp: ENSP00000393502.2:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-72G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.175G>A
  hgvsp: ENSP00000257857.4:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.175G>A
  hgvsp: ENSP00000449435.1:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.175G>A
  hgvsp: ENSP00000450191.1:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.175G>A
  hgvsp: ENSP00000449337.1:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.175G>A
  hgvsp: ENSP00000447730.1:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.106G>A
  hgvsp: ENSP00000446807.1:p.Ala36Thr
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-72G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.175G>A
  hgvsp: ENSP00000449281.1:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala59Thr
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

12-56121015-CGAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121015
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121012
    reference: chr 12
allele count: 4
allele frequency: 3.304692663582287e-5
allele num: 121040
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.172_174delATC
  hgvsp: ENSP00000447730.1:p.Ile58del
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.172_174delATC
  hgvsp: ENSP00000449435.1:p.Ile58del
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.103_105delATC
  hgvsp: ENSP00000446807.1:p.Ile35del
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.172_174delATC
  hgvsp: ENSP00000450191.1:p.Ile58del
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.172_174delATC
  hgvsp: ENSP00000257857.4:p.Ile58del
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.172_174delATC
  hgvsp: ENSP00000449281.1:p.Ile58del
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.172_174delATC
  hgvsp: ENSP00000449337.1:p.Ile58del
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.172_174delATC
  hgvsp: ENSP00000393502.2:p.Ile58del
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.172_174delATC
  hgvsp: ENSP00000446752.1:p.Ile58del
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-75_-73delATC
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-75_-73delATC
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile58del
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: CGAT
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum

12-56121022-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121022
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121022
    reference: chr 12
allele count: 3
allele frequency: 2.4786833234186e-5
allele num: 121032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.168C>T
  hgvsp: ENST00000546457.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-79C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.168C>T
  hgvsp: ENST00000420846.3:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.168C>T
  hgvsp: ENST00000552164.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-79C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.168C>T
  hgvsp: ENST00000549117.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.168C>T
  hgvsp: ENST00000550050.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.168C>T
  hgvsp: ENST00000551173.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.168C>T
  hgvsp: ENST00000257857.4:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.168C>T
  hgvsp: ENST00000552692.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.99C>T
  hgvsp: ENST00000552754.1:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11276
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6708
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8418
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val56Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

12-56121040-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121040
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121040
    reference: chr 12
allele count: 1
allele frequency: 8.26801600687899e-6
allele num: 120948
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.150C>T
  hgvsp: ENST00000546457.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.150C>T
  hgvsp: ENST00000552692.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.81C>T
  hgvsp: ENST00000552754.1:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.150C>T
  hgvsp: ENST00000257857.4:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.150C>T
  hgvsp: ENST00000549117.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-97C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-97C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.150C>T
  hgvsp: ENST00000552164.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.150C>T
  hgvsp: ENST00000550050.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.150C>T
  hgvsp: ENST00000551173.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.150C>T
  hgvsp: ENST00000420846.3:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10896
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly50Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

12-56121041-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121041
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121041
    reference: chr 12
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.149G>C
  hgvsp: ENSP00000450191.1:p.Gly50Ala
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.149G>C
  hgvsp: ENSP00000446752.1:p.Gly50Ala
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.149G>C
  hgvsp: ENSP00000447730.1:p.Gly50Ala
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.149G>C
  hgvsp: ENSP00000449435.1:p.Gly50Ala
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-98G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.80G>C
  hgvsp: ENSP00000446807.1:p.Gly27Ala
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.149G>C
  hgvsp: ENSP00000257857.4:p.Gly50Ala
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.149G>C
  hgvsp: ENSP00000449281.1:p.Gly50Ala
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-98G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.149G>C
  hgvsp: ENSP00000449337.1:p.Gly50Ala
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.149G>C
  hgvsp: ENSP00000393502.2:p.Gly50Ala
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly50Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/12-56121042-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121042
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121041
    reference: chr 12
allele count: 1
allele frequency: 8.267469162340024e-6
allele num: 120956
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.147delT
  hgvsp: ENSP00000446752.1:p.Gly50AlafsTer34
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-100delT
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.147delT
  hgvsp: ENSP00000447730.1:p.Gly50AlafsTer34
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.147delT
  hgvsp: ENSP00000449281.1:p.Gly50AlafsTer34
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.147delT
  hgvsp: ENSP00000257857.4:p.Gly50AlafsTer34
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.147delT
  hgvsp: ENSP00000393502.2:p.Gly50AlafsTer34
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-100delT
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.78delT
  hgvsp: ENSP00000446807.1:p.Gly27AlafsTer34
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.147delT
  hgvsp: ENSP00000450191.1:p.Gly50AlafsTer34
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.147delT
  hgvsp: ENSP00000449435.1:p.Gly50AlafsTer34
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.147delT
  hgvsp: ENSP00000449337.1:p.Gly50AlafsTer34
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly50AlafsTer34
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: CA
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS

http://identifiers.org/exac.variant/12-56121043-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121043
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121043
    reference: chr 12
allele count: 1
allele frequency: 8.273899157717065e-6
allele num: 120862
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.78T>G
  hgvsp: ENST00000552754.1:c.78T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.147T>G
  hgvsp: ENST00000549117.1:c.147T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.147T>G
  hgvsp: ENST00000546457.1:c.147T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.147T>G
  hgvsp: ENST00000550050.1:c.147T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-100T>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.147T>G
  hgvsp: ENST00000551173.1:c.147T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.147T>G
  hgvsp: ENST00000257857.4:c.147T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-100T>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.147T>G
  hgvsp: ENST00000552692.1:c.147T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.147T>G
  hgvsp: ENST00000420846.3:c.147T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.147T>G
  hgvsp: ENST00000552164.1:c.147T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11237
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro49Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-56121046-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121046
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121046
    reference: chr 12
allele count: 1
allele frequency: 8.268289456277286e-6
allele num: 120944
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.144C>G
  hgvsp: ENST00000550050.1:c.144C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.144C>G
  hgvsp: ENST00000549117.1:c.144C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.144C>G
  hgvsp: ENST00000552692.1:c.144C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.144C>G
  hgvsp: ENST00000551173.1:c.144C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.144C>G
  hgvsp: ENST00000546457.1:c.144C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.144C>G
  hgvsp: ENST00000257857.4:c.144C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-103C>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.144C>G
  hgvsp: ENST00000552164.1:c.144C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.144C>G
  hgvsp: ENST00000420846.3:c.144C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.75C>G
  hgvsp: ENST00000552754.1:c.75C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-103C>G
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr48Thr
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

12-56121051-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121051
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121051
    reference: chr 12
allele count: 1
allele frequency: 8.271298593879239e-6
allele num: 120900
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.139G>C
  hgvsp: ENSP00000449337.1:p.Ala47Pro
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-108G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.139G>C
  hgvsp: ENSP00000449435.1:p.Ala47Pro
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-108G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.139G>C
  hgvsp: ENSP00000393502.2:p.Ala47Pro
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.139G>C
  hgvsp: ENSP00000257857.4:p.Ala47Pro
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.139G>C
  hgvsp: ENSP00000449281.1:p.Ala47Pro
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.139G>C
  hgvsp: ENSP00000446752.1:p.Ala47Pro
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.139G>C
  hgvsp: ENSP00000447730.1:p.Ala47Pro
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.70G>C
  hgvsp: ENSP00000446807.1:p.Ala24Pro
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.139G>C
  hgvsp: ENSP00000450191.1:p.Ala47Pro
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6708
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6436
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala47Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

12-56121055-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121055
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121055
    reference: chr 12
allele count: 1
allele frequency: 8.272940865018697e-6
allele num: 120876
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.135G>C
  hgvsp: ENSP00000450191.1:p.Gln45His
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.67-1G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.135G>C
  hgvsp: ENSP00000446752.1:p.Gln45His
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.135G>C
  hgvsp: ENSP00000449281.1:p.Gln45His
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-112G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.135G>C
  hgvsp: ENSP00000447730.1:p.Gln45His
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.135G>C
  hgvsp: ENSP00000449435.1:p.Gln45His
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-112G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.135G>C
  hgvsp: ENSP00000449337.1:p.Gln45His
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.135G>C
  hgvsp: ENSP00000257857.4:p.Gln45His
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.135G>C
  hgvsp: ENSP00000393502.2:p.Gln45His
  variant of: http://identifiers.org/hgnc/1692
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.67-1G>C
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

12-56121079-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121079
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121080
    reference: chr 12
allele count: 7
allele frequency: 5.80113702285648e-5
allele num: 120666
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.110_111insA
  hgvsp: ENSP00000449281.1:p.Val38CysfsTer71
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.110_111insA
  hgvsp: ENSP00000449435.1:p.Val38CysfsTer202
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.110_111insA
  hgvsp: ENSP00000447730.1:p.Val38CysfsTer71
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.110_111insA
  hgvsp: ENSP00000257857.4:p.Val38CysfsTer71
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.110_111insA
  hgvsp: ENSP00000450191.1:p.Val38CysfsTer71
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.110_111insA
  hgvsp: ENSP00000446752.1:p.Val38CysfsTer71
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-137_-136insA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.110_111insA
  hgvsp: ENSP00000449337.1:p.Val38CysfsTer71
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.67-26_67-25insA
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.110_111insA
  hgvsp: ENSP00000393502.2:p.Val38CysfsTer71
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-137_-136insA
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5099
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10847
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8402
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val38CysfsTer71
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

12-56121081-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121081
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121081
    reference: chr 12
allele count: 1
allele frequency: 8.2917364554485e-6
allele num: 120602
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.67-27C>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.109C>G
  hgvsp: ENSP00000447730.1:p.Leu37Val
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.109C>G
  hgvsp: ENSP00000449281.1:p.Leu37Val
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.109C>G
  hgvsp: ENSP00000449337.1:p.Leu37Val
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.109C>G
  hgvsp: ENSP00000257857.4:p.Leu37Val
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.109C>G
  hgvsp: ENSP00000450191.1:p.Leu37Val
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-138C>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.109C>G
  hgvsp: ENSP00000449435.1:p.Leu37Val
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.109C>G
  hgvsp: ENSP00000393502.2:p.Leu37Val
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.109C>G
  hgvsp: ENSP00000446752.1:p.Leu37Val
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-138C>G
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu37Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

12-56121087-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121087
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121087
    reference: chr 12
allele count: 1
allele frequency: 8.301235223801302e-6
allele num: 120464
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-144G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.103G>A
  hgvsp: ENSP00000449337.1:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.103G>A
  hgvsp: ENSP00000393502.2:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.103G>A
  hgvsp: ENSP00000450191.1:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.103G>A
  hgvsp: ENSP00000257857.4:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.103G>A
  hgvsp: ENSP00000449281.1:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-144G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.103G>A
  hgvsp: ENSP00000449435.1:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.103G>A
  hgvsp: ENSP00000447730.1:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.103G>A
  hgvsp: ENSP00000446752.1:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.67-33G>A
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10836
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5099
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala35Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

12-56121088-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121088
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121088
    reference: chr 12
allele count: 1
allele frequency: 8.300408380092301e-6
allele num: 120476
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.102G>A
  hgvsp: ENST00000551173.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.102G>A
  hgvsp: ENST00000546457.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.102G>A
  hgvsp: ENST00000552164.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.102G>A
  hgvsp: ENST00000549117.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.102G>A
  hgvsp: ENST00000550050.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.102G>A
  hgvsp: ENST00000552692.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.102G>A
  hgvsp: ENST00000257857.4:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.102G>A
  hgvsp: ENST00000420846.3:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-145G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.67-34G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-145G>A
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly34Gly
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

12-56121096-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121096
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121096
    reference: chr 12
allele count: 1
allele frequency: 8.31849867735871e-6
allele num: 120214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.94G>A
  hgvsp: ENSP00000449281.1:p.Gly32Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.94G>A
  hgvsp: ENSP00000257857.4:p.Gly32Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.94G>A
  hgvsp: ENSP00000447730.1:p.Gly32Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.94G>A
  hgvsp: ENSP00000449435.1:p.Gly32Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.94G>A
  hgvsp: ENSP00000393502.2:p.Gly32Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-153G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-153G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.94G>A
  hgvsp: ENSP00000450191.1:p.Gly32Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.94G>A
  hgvsp: ENSP00000446752.1:p.Gly32Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.94G>A
  hgvsp: ENSP00000449337.1:p.Gly32Ser
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.67-42G>A
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10835
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly32Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

12-56121099-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121099
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121099
    reference: chr 12
allele count: 79
allele frequency: 6.573691918519504e-4
allele num: 120176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.91G>A
  hgvsp: ENSP00000449281.1:p.Val31Met
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-156G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.67-45G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.91G>A
  hgvsp: ENSP00000393502.2:p.Val31Met
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.91G>A
  hgvsp: ENSP00000257857.4:p.Val31Met
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.91G>A
  hgvsp: ENSP00000450191.1:p.Val31Met
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-156G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.91G>A
  hgvsp: ENSP00000449337.1:p.Val31Met
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.91G>A
  hgvsp: ENSP00000449435.1:p.Val31Met
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.91G>A
  hgvsp: ENSP00000446752.1:p.Val31Met
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.91G>A
  hgvsp: ENSP00000447730.1:p.Val31Met
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 9.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 8400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 10813
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3747
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: p.Val31Met
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

12-56121101-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121101
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121101
    reference: chr 12
allele count: 1
allele frequency: 8.328752519447637e-6
allele num: 120066
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.89C>A
  hgvsp: ENSP00000449281.1:p.Ala30Asp
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.89C>A
  hgvsp: ENSP00000449337.1:p.Ala30Asp
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.89C>A
  hgvsp: ENSP00000257857.4:p.Ala30Asp
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-158C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.89C>A
  hgvsp: ENSP00000449435.1:p.Ala30Asp
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.89C>A
  hgvsp: ENSP00000447730.1:p.Ala30Asp
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-158C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.89C>A
  hgvsp: ENSP00000450191.1:p.Ala30Asp
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.89C>A
  hgvsp: ENSP00000393502.2:p.Ala30Asp
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.67-47C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.89C>A
  hgvsp: ENSP00000446752.1:p.Ala30Asp
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11048
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5099
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5773
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala30Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

12-56121103-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121103
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121103
    reference: chr 12
allele count: 3
allele frequency: 2.500208350695891e-5
allele num: 119990
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.87T>C
  hgvsp: ENST00000549117.1:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.87T>C
  hgvsp: ENST00000257857.4:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-160T>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-160T>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.87T>C
  hgvsp: ENST00000546457.1:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.87T>C
  hgvsp: ENST00000550050.1:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.87T>C
  hgvsp: ENST00000420846.3:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.87T>C
  hgvsp: ENST00000552692.1:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.87T>C
  hgvsp: ENST00000551173.1:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.67-49T>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.87T>C
  hgvsp: ENST00000552164.1:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11027
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10811
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5097
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile29Ile
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

12-56121106-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121106
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121106
    reference: chr 12
allele count: 1
allele frequency: 8.342092530490349e-6
allele num: 119874
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.84G>C
  hgvsp: ENST00000257857.4:c.84G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.84G>C
  hgvsp: ENST00000551173.1:c.84G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-163G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.84G>C
  hgvsp: ENST00000546457.1:c.84G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.84G>C
  hgvsp: ENST00000550050.1:c.84G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.84G>C
  hgvsp: ENST00000552164.1:c.84G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.84G>C
  hgvsp: ENST00000552692.1:c.84G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-163G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.67-52G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.84G>C
  hgvsp: ENST00000420846.3:c.84G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.84G>C
  hgvsp: ENST00000549117.1:c.84G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5097
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6710
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu28Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

12-56121128-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121128
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121128
    reference: chr 12
allele count: 1
allele frequency: 8.471848048933394e-6
allele num: 118038
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-180-5C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.67-5C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.67-5C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.67-5C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.67-5C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.67-5C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.67-5C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.67-5C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.67-74C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-180-5C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.67-5C>A
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10568
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.67-5C>A
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP

12-56121133-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121133
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121133
    reference: chr 12
allele count: 1
allele frequency: 8.49689863199932e-6
allele num: 117690
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.67-10T>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.67-10T>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-180-10T>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.67-10T>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.67-10T>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.67-10T>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.67-10T>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.67-10T>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.67-10T>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-180-10T>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.67-79T>C
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5089
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3747
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6699
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

12-56121143-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121143
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121143
    reference: chr 12
allele count: 311
allele frequency: 2.661167490972567e-3
allele num: 116866
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.67-20C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.67-20C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.67-20C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-180-20C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.67-20C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.67-20C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.67-20C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.67-20C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-180-20C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.67-20C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.67-89C>T
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 3775
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 4.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 6.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 5.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 9292
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 8340
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 10351
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 7.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 5.25e1
  variant carriers: 32
genotype quality: GenotypeQuality
  all individuals: 917
  bin: 2.75e1
  variant carriers: 2
num of homozygotes: 4
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

12-56121154-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121154
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121154
    reference: chr 12
allele count: 1
allele frequency: 8.623068432671082e-6
allele num: 115968
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.67-31A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-180-31A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.67-31A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.67-31A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.67-31A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-180-31A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.67-31A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.67-31A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.67-31A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.67-31A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.67-100A>G
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8774
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

12-56121169-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121169
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121169
    reference: chr 12
allele count: 2
allele frequency: 1.758984010835342e-5
allele num: 113702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.67-46C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.67-46C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.67-46C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.67-46C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.67-46C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.67-115C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.67-46C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.67-46C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-180-46C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.67-46C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-180-46C>T
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6946
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3494
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

12-56121174-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121174
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121174
    reference: chr 12
allele count: 10
allele frequency: 8.828930639920892e-5
allele num: 113264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-180-51A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-180-51A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.67-51A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.67-51A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.67-51A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.67-51A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.67-51A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.67-51A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.67-51A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.67-120A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.67-51A>G
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6898
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6565
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8263
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/12-56121175-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56121175
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56121175
    reference: chr 12
allele count: 1
allele frequency: 8.834234425244708e-6
allele num: 113196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447356
  ensembl transcript: ENST00000546939
  gene symbol: CD63
  hgvsc: ENST00000546939.1:c.-180-52G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.67-52G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.67-52G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.67-52G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.67-52G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.67-52G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.67-52G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.67-52G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.67-52G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000448091
  ensembl transcript: ENST00000550776
  gene symbol: CD63
  hgvsc: ENST00000550776.1:c.-180-52G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.67-121G>T
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6928
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3078
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7893
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

12-56122010-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56122010
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56122010
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 63938
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.66+50C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.66+50C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.66+50C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.66+50C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.66+50C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.66+50C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.66+50C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.66+50C>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.66+50C>A
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16666
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22008
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3074
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4222
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

12-56122013-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56122013
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56122013
    reference: chr 12
allele count: 38
allele frequency: 5.935088870146503e-4
allele num: 64026
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.66+47G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.66+47G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.66+47G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.66+47G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.66+47G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.66+47G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.66+47G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.66+47G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.66+47G>C
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6052
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16684
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21983
  bin: 7.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5123
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2869
  bin: 9.75e1
  variant carriers: 40
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1258
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4196
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

12-56122017-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56122017
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56122017
    reference: chr 12
allele count: 1
allele frequency: 1.56011107990889e-5
allele num: 64098
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.66+43G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.66+43G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.66+43G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.66+43G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.66+43G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.66+43G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.66+43G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.66+43G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.66+43G>A
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5827
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16680
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22034
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4585
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2836
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6778
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1270
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

12-56122018-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56122018
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56122018
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 64168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.66+42G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.66+42G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.66+42G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.66+42G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.66+42G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.66+42G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.66+42G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.66+42G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.66+42G>A
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22024
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5723
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2836
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18252
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1421
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3649
  bin: 1.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

12-56122020-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56122020
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56122020
    reference: chr 12
allele count: 114
allele frequency: 1.75465599507465e-3
allele num: 64970
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.66+40G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.66+40G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.66+40G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.66+40G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.66+40G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.66+40G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.66+40G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.66+40G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.66+40G>C
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22003
  bin: 7.5e0
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 16627
  bin: 1.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4289
  bin: 1.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5508
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2443
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 5.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4558
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1298
  bin: 4.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum

12-56122025-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56122025
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56122025
    reference: chr 12
allele count: 8
allele frequency: 1.21311375974282e-4
allele num: 65946
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.66+35A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.66+35A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.66+35A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.66+35A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.66+35A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.66+35A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.66+35A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.66+35A>G
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.66+35A>G
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16104
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22304
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21095
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4193
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

12-56122029-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56122029
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56122029
    reference: chr 12
allele count: 2
allele frequency: 2.991146207226609e-5
allele num: 66864
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.66+31C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.66+31C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.66+31C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.66+31C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.66+31C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.66+31C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.66+31C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.66+31C>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.66+31C>T
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6266
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2825
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3883
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

12-56122033-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56122033
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56122033
    reference: chr 12
allele count: 1
allele frequency: 1.469896519285042e-5
allele num: 68032
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.66+27G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.66+27G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.66+27G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.66+27G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.66+27G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.66+27G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.66+27G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.66+27G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.66+27G>C
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1271
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21995
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5771
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD

12-56122034-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56122034
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56122033
    reference: chr 12
allele count: 7
allele frequency: 1.032966384322522e-4
allele num: 67766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.66+25delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.66+25delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.66+25delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.66+25delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.66+25delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.66+25delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.66+25delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.66+25delG
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.66+25delG
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8230
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14146
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2046
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3234
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3558
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4535
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3000
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: GC
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

12-56122035-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56122035
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56122035
    reference: chr 12
allele count: 2
allele frequency: 2.941003470384095e-5
allele num: 68004
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.66+25G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.66+25G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.66+25G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.66+25G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.66+25G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.66+25G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.66+25G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.66+25G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.66+25G>C
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21857
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1782
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1227
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/12-56122037-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56122037
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56122037
    reference: chr 12
allele count: 2
allele frequency: 2.854777470096206e-5
allele num: 70058
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.66+23G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.66+23G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.66+23G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.66+23G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.66+23G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.66+23G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.66+23G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.66+23G>T
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.66+23G>T
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13333
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21824
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9431
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2851
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21986
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10661
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1238
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

12-56122059-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56122059
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56122059
    reference: chr 12
allele count: 1
allele frequency: 1.254988579603926e-5
allele num: 79682
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.66+1G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.66+1G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.66+1G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.66+1G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.66+1G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.66+1G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.66+1G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.66+1G>C
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.66+1G>C
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18766
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7960
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2600
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 5.75e1
  variant carriers: 0
hgvs: c.66+1G>C
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP

12-56122059-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56122059
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56122059
    reference: chr 12
allele count: 2
allele frequency: 2.509977159207851e-5
allele num: 79682
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.66+1G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.66+1G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.66+1G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.66+1G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.66+1G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.66+1G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.66+1G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.66+1G>A
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.66+1G>A
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7960
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19091
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18766
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1735
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2825
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2035
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20194
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 1.25e1
  variant carriers: 0
hgvs: c.66+1G>A
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-56122066-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56122066
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56122066
    reference: chr 12
allele count: 3
allele frequency: 3.621701233792887e-5
allele num: 82834
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.60C>T
  hgvsp: ENST00000546457.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.60C>T
  hgvsp: ENST00000550050.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.60C>T
  hgvsp: ENST00000549117.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.60C>T
  hgvsp: ENST00000551173.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.60C>T
  hgvsp: ENST00000552692.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.60C>T
  hgvsp: ENST00000257857.4:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.60C>T
  hgvsp: ENST00000552754.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.60C>T
  hgvsp: ENST00000552164.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.60C>T
  hgvsp: ENST00000420846.3:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17545
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7000
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala20Ala
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

12-56122077-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56122077
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56122077
    reference: chr 12
allele count: 2
allele frequency: 2.305209774089442e-5
allele num: 86760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.49C>T
  hgvsp: ENSP00000450191.1:p.Leu17Phe
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.49C>T
  hgvsp: ENSP00000393502.2:p.Leu17Phe
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.49C>T
  hgvsp: ENSP00000447730.1:p.Leu17Phe
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.49C>T
  hgvsp: ENSP00000449435.1:p.Leu17Phe
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.49C>T
  hgvsp: ENSP00000446807.1:p.Leu17Phe
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.49C>T
  hgvsp: ENSP00000257857.4:p.Leu17Phe
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.49C>T
  hgvsp: ENSP00000449337.1:p.Leu17Phe
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.49C>T
  hgvsp: ENSP00000449281.1:p.Leu17Phe
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.49C>T
  hgvsp: ENSP00000446752.1:p.Leu17Phe
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15801
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1660
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu17Phe
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

12-56122084-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56122084
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 56122084
    reference: chr 12
allele count: 702
allele frequency: 7.8397212543554e-3
allele num: 89544
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000450191
  ensembl transcript: ENST00000546457
  gene symbol: CD63
  hgvsc: ENST00000546457.1:c.42C>G
  hgvsp: ENST00000546457.1:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000257857
  ensembl transcript: ENST00000257857
  gene symbol: CD63
  hgvsc: ENST00000257857.4:c.42C>G
  hgvsp: ENST00000257857.4:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449281
  ensembl transcript: ENST00000552164
  gene symbol: CD63
  hgvsc: ENST00000552164.1:c.42C>G
  hgvsp: ENST00000552164.1:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446807
  ensembl transcript: ENST00000552754
  gene symbol: CD63
  hgvsc: ENST00000552754.1:c.42C>G
  hgvsp: ENST00000552754.1:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449337
  ensembl transcript: ENST00000552692
  gene symbol: CD63
  hgvsc: ENST00000552692.1:c.42C>G
  hgvsp: ENST00000552692.1:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000449435
  ensembl transcript: ENST00000550050
  gene symbol: CD63
  hgvsc: ENST00000550050.1:c.42C>G
  hgvsp: ENST00000550050.1:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000393502
  ensembl transcript: ENST00000420846
  gene symbol: CD63
  hgvsc: ENST00000420846.3:c.42C>G
  hgvsp: ENST00000420846.3:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000447730
  ensembl transcript: ENST00000549117
  gene symbol: CD63
  hgvsc: ENST00000549117.1:c.42C>G
  hgvsp: ENST00000549117.1:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135404
  ensembl protein: ENSP00000446752
  ensembl transcript: ENST00000551173
  gene symbol: CD63
  hgvsc: ENST00000551173.1:c.42C>G
  hgvsp: ENST00000551173.1:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1692
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 5954
  bin: 2.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 1.75e1
  variant carriers: 159
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 14500
  bin: 7.5e0
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 3.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 25130
  bin: 2.25e1
  variant carriers: 148
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 3.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5400
  bin: 1.25e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 4.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 5.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1273
  bin: 3.25e1
  variant carriers: 2
hgvs: p.Leu14Leu
num of homozygotes: 1
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD

GenotypeDepth
all individuals: 3754
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2587
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2119
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10890
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3832
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5217
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22141
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1069
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3538
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4193
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1974
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13812
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.326663564448581e-4
allele num: 8596
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.969e1

MQRankSum
type: SiteQuality
SIO_000300: 2.57e-1

FS
type: SiteQuality
SIO_000300: 7.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.888e0

DP
type: SiteQuality
SIO_000300: 2.278572e6

VQSLOD
type: SiteQuality
SIO_000300: 7.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

QD
type: SiteQuality
SIO_000300: 1.166e1

GenotypeDepth
all individuals: 377
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11226
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3833
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4191
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2590
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1050
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22137
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3538
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 857
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5232
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.939487975174554e-4
allele num: 10312
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13922
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.528e0

MQRankSum
type: SiteQuality
SIO_000300: -5.497e0

MQ
type: SiteQuality
SIO_000300: 5.458e1

VQSLOD
type: SiteQuality
SIO_000300: 6.5e-2

FS
type: SiteQuality
SIO_000300: 1.607e0

QD
type: SiteQuality
SIO_000300: 1.123e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

DP
type: SiteQuality
SIO_000300: 2.279886e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

GenotypeDepth
all individuals: 5103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2204
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5241
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3537
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3832
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1050
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22137
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 174
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4192
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2589
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11182
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1970
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.174630506528914e-5
allele num: 13938
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65500
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.36e-1

MQ
type: SiteQuality
SIO_000300: 5.446e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.705e0

FS
type: SiteQuality
SIO_000300: 3.377e0

MQRankSum
type: SiteQuality
SIO_000300: -6.078e0

DP
type: SiteQuality
SIO_000300: 2.280034e6

QD
type: SiteQuality
SIO_000300: 9.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.717e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

GenotypeDepth
all individuals: 698
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5241
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4192
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2204
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22137
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1970
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3832
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11182
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3537
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2589
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1050
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65500
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.940240589833139e-4
allele num: 10308
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13938
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -6.078e0

MQ
type: SiteQuality
SIO_000300: 5.446e1

DP
type: SiteQuality
SIO_000300: 2.280034e6

VQSLOD
type: SiteQuality
SIO_000300: 8.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.705e0

FS
type: SiteQuality
SIO_000300: 3.377e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

QD
type: SiteQuality
SIO_000300: 9.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.717e0

GenotypeDepth
all individuals: 3753
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3827
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2593
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2196
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1040
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11270
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5231
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1971
bin: 8.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 175
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3538
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4196
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22136
bin: 9.75e1
variant carriers: 3

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.184940364994971e-5
allele num: 13918
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.053901358986105e-5
allele num: 65490
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

DP
type: SiteQuality
SIO_000300: 2.280658e6

QD
type: SiteQuality
SIO_000300: 1.202e1

FS
type: SiteQuality
SIO_000300: 2.777e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 698
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2593
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22136
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 112
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65490
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.184940364994971e-5
allele num: 13918
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

DP
type: SiteQuality
SIO_000300: 2.280658e6

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

FS
type: SiteQuality
SIO_000300: 2.777e0

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

QD
type: SiteQuality
SIO_000300: 1.202e1

GenotypeDepth
all individuals: 5103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3534
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.735207357279195e-4
allele num: 11526
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14016
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

FS
type: SiteQuality
SIO_000300: 5.357e0

VQSLOD
type: SiteQuality
SIO_000300: 3.17e-1

QD
type: SiteQuality
SIO_000300: 1.336e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.42e0

DP
type: SiteQuality
SIO_000300: 2.282206e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.79e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

GenotypeDepth
all individuals: 9805
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 843
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3535
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14104
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.939864209505335e-4
allele num: 10310
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65562
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.53e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.533e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.442e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

QD
type: SiteQuality
SIO_000300: 4.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 5.416e1

DP
type: SiteQuality
SIO_000300: 2.282818e6

MQRankSum
type: SiteQuality
SIO_000300: -6.991e0

FS
type: SiteQuality
SIO_000300: 1.0304e1

GenotypeDepth
all individuals: 2516
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1970
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
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variant carriers: 0

GenotypeQuality
all individuals: 2601
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 4.25e1
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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 22129
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 232
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65614
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.407459535538353e-4
allele num: 14210
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.742000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.03e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.76e0

DP
type: SiteQuality
SIO_000300: 2.284661e6

VQSLOD
type: SiteQuality
SIO_000300: 9.330000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.243e0

QD
type: SiteQuality
SIO_000300: 1.198e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 1987
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.386962552011096e-4
allele num: 14420
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65656
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 8.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.43e-1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: 5.649999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

DP
type: SiteQuality
SIO_000300: 2.292135e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65672
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.378169790518192e-4
allele num: 14512
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 8.72e-1

MQRankSum
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VQSLOD
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QD
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.29457e6

MQ
type: SiteQuality
SIO_000300: 6.006e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.38e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3826
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65672
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.322880371660859e-4
allele num: 8610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14512
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.006e1

QD
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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SIO_000300: 3.1e-3

ReadPosRankSum
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SIO_000300: 3.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.33e0

BaseQRankSum
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SIO_000300: 8.72e-1

DP
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

East Asian
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South Asian
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Other
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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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: 4.568156900962358e-5
allele num: 65672
num of homozygotes: 0

ClippingRankSum
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FS
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QD
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DP
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQRankSum
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SIO_000300: 4.33e-1

MQ
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SIO_000300: 6.006e1

BaseQRankSum
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SIO_000300: 8.72e-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

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

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

Other
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.031313468125739e-5
allele num: 65978
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QD
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FS
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ClippingRankSum
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VQSLOD
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MQRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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variant carriers: 0

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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South Asian
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European (Finnish)
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African
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Latino
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European (Non-Finnish)
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DP
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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FS
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VQSLOD
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MQ
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QD
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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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European (Non-Finnish)
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allele frequency: 1.50993537476596e-5
allele num: 66228
num of homozygotes: 0

African
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East Asian
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South Asian
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Other
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Latino
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European (Finnish)
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BaseQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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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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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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Latino
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allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

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

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

South Asian
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African
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Latino
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European (Finnish)
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East Asian
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allele num: 8644
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Other
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European (Non-Finnish)
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MQRankSum
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QD
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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BaseQRankSum
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FS
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ReadPosRankSum
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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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bin: 2.75e1
variant carriers: 0

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

European (Finnish)
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num of homozygotes: 0

East Asian
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Latino
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African
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South Asian
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Other
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European (Non-Finnish)
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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MQRankSum
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FS
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QD
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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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bin: 9.25e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.00833308263891e-5
allele num: 66482
num of homozygotes: 0

South Asian
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ClippingRankSum
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QD
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InbreedingCoeff
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FS
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BaseQRankSum
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DP
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MQRankSum
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VQSLOD
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MQ
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SIO_000300: 5.806e1

ReadPosRankSum
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SIO_000300: 5.87e-1

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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variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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Latino
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num of homozygotes: 0

South Asian
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allele frequency: 1.212415130940834e-4
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num of homozygotes: 0

European (Finnish)
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European (Non-Finnish)
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Other
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MQ
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VQSLOD
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ClippingRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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FS
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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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variant carriers: 0

Other
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66484
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East Asian
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allele num: 8648
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South Asian
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: -8.49e-1

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505389293671343e-5
allele num: 66428
num of homozygotes: 0

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

African
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QD
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InbreedingCoeff
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VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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MQ
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SIO_000300: 5.979e1

MQRankSum
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SIO_000300: 9.12e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 1.22e0

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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European (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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African
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Other
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East Asian
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European (Non-Finnish)
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ReadPosRankSum
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MQ
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DP
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MQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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VQSLOD
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QD
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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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bin: 8.25e1
variant carriers: 0

European (Finnish)
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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South Asian
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East Asian
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Other
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Latino
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African
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DP
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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QD
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MQRankSum
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MQ
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FS
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BaseQRankSum
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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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South Asian
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Other
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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Latino
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DP
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ClippingRankSum
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SIO_000300: 2.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.73e-1

FS
type: SiteQuality
SIO_000300: 5.745e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
type: SiteQuality
SIO_000300: 9.56e0

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66396
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.708737864077671e-5
allele num: 10300
num of homozygotes: 0

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.114e1

MQRankSum
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SIO_000300: 5.49e-1

DP
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InbreedingCoeff
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SIO_000300: -2.0e-4

VQSLOD
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FS
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SIO_000300: 4.36e-1

MQ
type: SiteQuality
SIO_000300: 5.986e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.94e-1

BaseQRankSum
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SIO_000300: 1.97e0

ClippingRankSum
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SIO_000300: 1.91e0

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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506341698550899e-5
allele num: 66386
num of homozygotes: 0

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

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

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

InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
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SIO_000300: -5.509e0

DP
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SIO_000300: 2.337274e6

MQRankSum
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FS
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MQ
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ClippingRankSum
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SIO_000300: -2.039e0

ReadPosRankSum
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SIO_000300: 3.46e0

VQSLOD
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SIO_000300: -2.256e0

QD
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SIO_000300: 1.327e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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 count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 1.056444310292786e-4
allele num: 66260
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 1.44e0

DP
type: SiteQuality
SIO_000300: 2.333867e6

MQRankSum
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SIO_000300: 1.43e-1

MQ
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.26e-1

QD
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SIO_000300: 1.473e1

VQSLOD
type: SiteQuality
SIO_000300: 5.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 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: 8634
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66228
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.750390015600624e-5
allele num: 10256
num of homozygotes: 0

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

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

Other
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num of homozygotes: 0

ClippingRankSum
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SIO_000300: 2.98e0

MQ
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DP
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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FS
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SIO_000300: 2.595e0

BaseQRankSum
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SIO_000300: 1.37e0

MQRankSum
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SIO_000300: 6.22e-1

QD
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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
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66146
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

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

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

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

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

East Asian
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allele num: 8634
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

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

Latino
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allele 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

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

European (Non-Finnish)
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allele frequency: 1.511578692786746e-5
allele num: 66156
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QD
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BaseQRankSum
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ClippingRankSum
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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DP
type: SiteQuality
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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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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514187941007238e-5
allele num: 66042
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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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 frequency: 0.0e0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

MQ
type: SiteQuality
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FS
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InbreedingCoeff
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MQRankSum
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DP
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ReadPosRankSum
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QD
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 8

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 78

GenotypeQuality
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GenotypeQuality
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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: 5410
bin: 6.75e1
variant carriers: 1

East Asian
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allele count: 75
allele frequency: 8.686587908269632e-3
allele num: 8634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.155361319709468e-5
allele num: 16246
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.732801940738174e-4
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66020
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.174e1

VQSLOD
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InbreedingCoeff
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SIO_000300: -1.0e-3

DP
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SIO_000300: 2.327334e6

FS
type: SiteQuality
SIO_000300: 2.141e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ReadPosRankSum
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SIO_000300: 5.3e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e0

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
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65974
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.17283950617284e-5
allele num: 16200
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

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

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

VQSLOD
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SIO_000300: 1.35e-1

BaseQRankSum
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SIO_000300: -3.696e0

DP
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SIO_000300: 2.32041e6

ClippingRankSum
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SIO_000300: 6.63e-1

FS
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SIO_000300: 0.0e0

MQ
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SIO_000300: 5.917e1

InbreedingCoeff
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SIO_000300: -4.0e-4

QD
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SIO_000300: 1.504e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.91e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

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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variant carriers: 3

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.856435643564356e-4
allele num: 16160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65938
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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.441e1

VQSLOD
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SIO_000300: -1.38e0

BaseQRankSum
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SIO_000300: 3.09e0

ClippingRankSum
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SIO_000300: -7.16e-1

ReadPosRankSum
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SIO_000300: 1.02e0

DP
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SIO_000300: 2.318521e6

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

FS
type: SiteQuality
SIO_000300: 7.713e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.866e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 1969
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variant carriers: 0

GenotypeQuality
all individuals: 85
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65888
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16100
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.74e0

MQ
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SIO_000300: 5.977e1

VQSLOD
type: SiteQuality
SIO_000300: 5.7e-2

BaseQRankSum
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InbreedingCoeff
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SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e-1

QD
type: SiteQuality
SIO_000300: 1.323e1

FS
type: SiteQuality
SIO_000300: 1.051e0

DP
type: SiteQuality
SIO_000300: 2.317095e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.34e-1

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
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GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.161710037174721e-4
allele num: 8608
num of homozygotes: 0

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

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

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

South Asian
type: Population
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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BaseQRankSum
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SIO_000300: -2.853e0

MQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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SIO_000300: 5.966e1

ReadPosRankSum
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FS
type: SiteQuality
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QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

DP
type: SiteQuality
SIO_000300: 2.279895e6

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65088
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.865824782951855e-5
allele num: 10136
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.956e1

MQRankSum
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VQSLOD
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DP
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ClippingRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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QD
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ReadPosRankSum
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SIO_000300: 2.15e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4
allele frequency: 6.175889328063241e-5
allele num: 64768
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14436
num of homozygotes: 0

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

African
type: Population
allele count: 299
allele frequency: 2.959809938626015e-2
allele num: 10102
num of homozygotes: 4

Latino
type: Population
allele count: 7
allele frequency: 6.089074460681977e-4
allele num: 11496
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.160092807424594e-3
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East Asian
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VQSLOD
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FS
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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QD
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.164144353899884e-4
allele num: 8590
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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DP
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QD
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FS
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MQRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

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
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variant carriers: 2

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 63504
num of homozygotes: 0

Other
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num of homozygotes: 0

South Asian
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allele frequency: 1.557632398753894e-4
allele num: 12840
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.578631642092634e-4
allele num: 63346
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
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DP
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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QD
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MQ
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BaseQRankSum
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VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e-1

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.580078371887246e-5
allele num: 63288
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.460000000000001e0

FS
type: SiteQuality
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BaseQRankSum
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.162212e6

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4968
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1752
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10968
num of homozygotes: 0

DP
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.21e-2

FS
type: SiteQuality
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VQSLOD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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East Asian
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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: 4.334633723450368e-4
allele num: 4614
num of homozygotes: 0

South Asian
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allele frequency: 3.099927060539752e-3
allele num: 10968
num of homozygotes: 1

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 5.633802816901409e-5
allele num: 35500
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

QD
type: SiteQuality
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VQSLOD
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BaseQRankSum
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FS
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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East Asian
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.815632391035027e-5
allele num: 35516
num of homozygotes: 0

Latino
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VQSLOD
type: SiteQuality
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QD
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MQ
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FS
type: SiteQuality
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ReadPosRankSum
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DP
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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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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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 35532
num of homozygotes: 0

African
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East Asian
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Latino
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European (Finnish)
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South Asian
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Other
type: Population
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MQ
type: SiteQuality
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FS
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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QD
type: SiteQuality
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 637
bin: 8.25e1
variant carriers: 5

Latino
type: Population
allele count: 6
allele frequency: 1.269572577232332e-3
allele num: 4726
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 2.762430939226519e-3
allele num: 1810
num of homozygotes: 0

African
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allele count: 6
allele frequency: 1.023541453428864e-3
allele num: 5862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 97
allele frequency: 2.695642507781236e-3
allele num: 35984
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 11040
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-2

QD
type: SiteQuality
SIO_000300: 1.364e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.42e-1

DP
type: SiteQuality
SIO_000300: 8.54861e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.7e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 7

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
all individuals: 631
bin: 8.25e1
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GenotypeQuality
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variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 420
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5936
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1868
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.004141905276428e-5
allele num: 11106
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 1.343054489639294e-3
allele num: 5212
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4832
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.186e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.67e-1

FS
type: SiteQuality
SIO_000300: 2.941e0

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

DP
type: SiteQuality
SIO_000300: 8.73031e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.04e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.390254420008625e-5
allele num: 37104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1906
num of homozygotes: 0

Other
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: 5984
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4970
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11180
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.169e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-2

QD
type: SiteQuality
SIO_000300: 1.236e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.92794e5

MQRankSum
type: SiteQuality
SIO_000300: -3.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.3e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11300
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5086
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.647989452867502e-4
allele num: 6068
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1976
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37756
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.91e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.501e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.4e-3

FS
type: SiteQuality
SIO_000300: 3.274e0

DP
type: SiteQuality
SIO_000300: 9.15864e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.956e0

QD
type: SiteQuality
SIO_000300: 1.037e1

GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 510
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5080
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.86219739292365e-4
allele num: 5370
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.064906022043555e-4
allele num: 37562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 5.060728744939271e-4
allele num: 1976
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6066
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.873114463176575e-5
allele num: 11270
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.24e-1

QD
type: SiteQuality
SIO_000300: 2.65e0

MQRankSum
type: SiteQuality
SIO_000300: 2.87e-1

DP
type: SiteQuality
SIO_000300: 9.27315e5

BaseQRankSum
type: SiteQuality
SIO_000300: -9.78e-1

FS
type: SiteQuality
SIO_000300: 2.162e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.262e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.96e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 511
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5120
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.773049645390071e-4
allele num: 11280
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37752
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6026
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1976
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5400
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -3.434e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.8e-3

QD
type: SiteQuality
SIO_000300: 3.216e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.32008e5

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: -1.537e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.564234063285297e-5
allele num: 38998
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6148
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.794687724335966e-4
allele num: 5572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2084
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.884e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.107e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.399999999999999e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.103e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.35e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.74e-1

QD
type: SiteQuality
SIO_000300: 1.7e0

DP
type: SiteQuality
SIO_000300: 9.46e5

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12114
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 540
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6754
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2536
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.238238058999955e-5
allele num: 44678
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 5.8e0

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.53e-1

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.883e1

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.85e0

FS
type: SiteQuality
SIO_000300: 1.2542e1

DP
type: SiteQuality
SIO_000300: 1.085885e6

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 540
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6754
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12114
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.47647611799991e-5
allele num: 44678
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6738
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2536
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 19283
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GenotypeQuality
all individuals: 824
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GenotypeQuality
all individuals: 1108
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GenotypeQuality
all individuals: 717
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22926
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1471
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2824
bin: 9.75e1
variant carriers: 2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2686
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.434454358270419e-5
allele num: 46624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12336
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.121255e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.46e-1

FS
type: SiteQuality
SIO_000300: 9.904e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -5.332e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.88e-1

MQ
type: SiteQuality
SIO_000300: 5.898e1

QD
type: SiteQuality
SIO_000300: 1.112e1

GenotypeQuality
all individuals: 17697
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1286
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26081
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 372
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1778
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2824
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2354
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2880
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7742
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6782
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.082299150881777e-5
allele num: 48992
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.735e0

DP
type: SiteQuality
SIO_000300: 1.167612e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.475e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

QD
type: SiteQuality
SIO_000300: 6.41e0

GenotypeQuality
all individuals: 16558
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27965
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 459
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1207
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 651
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 310
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 680
bin: 8.25e1
variant carriers: 9

GenotypeQuality
all individuals: 825
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 95
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1515
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2427
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 738
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 315
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 480
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 520
bin: 9.25e1
variant carriers: 10

GenotypeQuality
all individuals: 149
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3439
bin: 9.75e1
variant carriers: 674

European (Non-Finnish)
type: Population
allele count: 575
allele frequency: 1.136947838810456e-2
allele num: 50574
num of homozygotes: 1

South Asian
type: Population
allele count: 50
allele frequency: 3.89347453667653e-3
allele num: 12842
num of homozygotes: 0

Other
type: Population
allele count: 8
allele frequency: 1.346801346801347e-2
allele num: 594
num of homozygotes: 0

Latino
type: Population
allele count: 45
allele frequency: 5.509304603330069e-3
allele num: 8168
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.358695652173913e-3
allele num: 7360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 14
allele frequency: 4.60223537146614e-3
allele num: 3042
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6964
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.98e0