5-75003539-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003539
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003539
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 19896
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.358T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-1927T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-129+23T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.362+23T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-129+23T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.223+23T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.148+23T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.223+23T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.426+23T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-129+23T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.207+23T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-1927T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.*105+23T>C
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32414
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ

5-75003544-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003544
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003544
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 20368
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-1932A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-129+18A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-129+18A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.353A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.*105+18A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.223+18A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-129+18A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.223+18A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.362+18A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.207+18A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-1932A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.148+18A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.426+18A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33858
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/5-75003561-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003561
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003561
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 22244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-129+1G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.362+1G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.148+1G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.223+1G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-129+1G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.336G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-129+1G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.223+1G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.207+1G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.426+1G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-1949G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-1949G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.*105+1G>T
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: splice donor
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33923
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10392
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.223+1G>T
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

5-75003572-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003572
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003572
    reference: chr 5
allele count: 1
allele frequency: 4.2647560559536e-5
allele num: 23448
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-1960T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.213T>C
  hgvsp: ENST00000428202.2:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.197T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-139T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.*95T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-139T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.325T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.138T>C
  hgvsp: ENST00000446329.2:c.138T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.213T>C
  hgvsp: ENST00000514838.2:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-1960T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-139T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.352T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.416T>C
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17933
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28473
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu71Leu
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

5-75003587-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003587
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003587
    reference: chr 5
allele count: 2
allele frequency: 7.892036934732854e-5
allele num: 25342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.*80A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.401A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-154A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-1975A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.123A>C
  hgvsp: ENST00000446329.2:c.123A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.198A>C
  hgvsp: ENST00000428202.2:c.198A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-154A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-154A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-1975A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.198A>C
  hgvsp: ENST00000514838.2:c.198A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.337A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.182A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.310A>C
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25693
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20994
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr66Thr
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS

5-75003592-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003592
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003592
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 26308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-159T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.332T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-159T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-1980T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-159T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.193T>A
  hgvsp: ENSP00000410216.2:p.Ser65Thr
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.193T>A
  hgvsp: ENSP00000420971.1:p.Ser65Thr
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.396T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.177T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.118T>A
  hgvsp: ENSP00000399481.2:p.Ser40Thr
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-1980T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.*75T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.305T>A
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27800
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18594
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser65Thr
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum

5-75003597-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003597
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003597
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 27060
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.113G>C
  hgvsp: ENSP00000399481.2:p.Arg38Thr
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-164G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-164G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.391G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-164G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.188G>C
  hgvsp: ENSP00000410216.2:p.Arg63Thr
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-1985G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.300G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.*70G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.188G>C
  hgvsp: ENSP00000420971.1:p.Arg63Thr
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-1985G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.327G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.172G>C
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29856
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16241
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg63Thr
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

5-75003622-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003622
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003622
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 35550
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.163A>G
  hgvsp: ENSP00000410216.2:p.Lys55Glu
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.88A>G
  hgvsp: ENSP00000399481.2:p.Lys30Glu
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-189A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-189A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.163A>G
  hgvsp: ENSP00000420971.1:p.Lys55Glu
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.*45A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-189A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.366A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2010A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2010A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.147A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.275A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.302A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 7555
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34730
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys55Glu
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

5-75003624-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003624
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003624
    reference: chr 5
allele count: 2
allele frequency: 5.517545795630104e-5
allele num: 36248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-191C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.161C>T
  hgvsp: ENSP00000410216.2:p.Pro54Leu
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.145C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.364C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.161C>T
  hgvsp: ENSP00000420971.1:p.Pro54Leu
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.300C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-191C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.273C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-191C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.*43C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2012C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2012C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.86C>T
  hgvsp: ENSP00000399481.2:p.Pro29Leu
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34775
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7079
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro54Leu
num of homozygotes: 1
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

5-75003627-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003627
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003627
    reference: chr 5
allele count: 1
allele frequency: 2.668232029457282e-5
allele num: 37478
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2015A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.361A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.297A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.158A>G
  hgvsp: ENSP00000420971.1:p.His53Arg
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.83A>G
  hgvsp: ENSP00000399481.2:p.His28Arg
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.158A>G
  hgvsp: ENSP00000410216.2:p.His53Arg
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2015A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-194A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.*40A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.142A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-194A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.270A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-194A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34788
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9905
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6564
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His53Arg
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

5-75003635-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003635
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003635
    reference: chr 5
allele count: 1
allele frequency: 2.486201581224206e-5
allele num: 40222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2023G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.75G>A
  hgvsp: ENST00000446329.2:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.262G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.150G>A
  hgvsp: ENST00000514838.2:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2023G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.150G>A
  hgvsp: ENST00000428202.2:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.134G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.353G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-202G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.*32G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.289G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-202G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-202G>A
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10443
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln50Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

5-75003648-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003648
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003648
    reference: chr 5
allele count: 1
allele frequency: 2.199058802832388e-5
allele num: 45474
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-215C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.340C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.121C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.137C>T
  hgvsp: ENSP00000410216.2:p.Pro46Leu
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2036C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.276C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.62C>T
  hgvsp: ENSP00000399481.2:p.Pro21Leu
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.137C>T
  hgvsp: ENSP00000420971.1:p.Pro46Leu
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.*19C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-215C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2036C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.249C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-215C>T
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro46Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum

5-75003652-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003652
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003652
    reference: chr 5
allele count: 6
allele frequency: 1.273723092599669e-4
allele num: 47106
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.117G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.133G>A
  hgvsp: ENSP00000420971.1:p.Glu45Lys
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.133G>A
  hgvsp: ENSP00000410216.2:p.Glu45Lys
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-219G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.*15G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.272G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.336G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-219G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.58G>A
  hgvsp: ENSP00000399481.2:p.Glu20Lys
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-219G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2040G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2040G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.245G>A
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 32534
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Glu45Lys
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP

5-75003659-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003659
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003659
    reference: chr 5
allele count: 214
allele frequency: 4.330405924966611e-3
allele num: 49418
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2047A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.126A>G
  hgvsp: ENST00000514838.2:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2047A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-226A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.51A>G
  hgvsp: ENST00000446329.2:c.51A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-226A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.265A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-226A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.*8A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.110A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.126A>G
  hgvsp: ENST00000428202.2:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.238A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.329A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 1.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 31915
  bin: 7.5e0
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 5180
  bin: 1.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 12877
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 2.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Pro42Pro
num of homozygotes: 5
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

5-75003662-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003662
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003662
    reference: chr 5
allele count: 1
allele frequency: 1.980041184856645e-5
allele num: 50504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.48T>A
  hgvsp: ENST00000446329.2:c.48T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-229T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.326T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.107T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-229T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.262T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2050T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2050T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.*5T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.123T>A
  hgvsp: ENST00000514838.2:c.123T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.123T>A
  hgvsp: ENST00000428202.2:c.123T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-229T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.235T>A
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31528
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr41Thr
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/5-75003666-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003666
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003666
    reference: chr 5
allele count: 1
allele frequency: 1.928045347626576e-5
allele num: 51866
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.119T>G
  hgvsp: ENSP00000410216.2:p.Val40Gly
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.44T>G
  hgvsp: ENSP00000399481.2:p.Val15Gly
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-233T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-233T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.119T>G
  hgvsp: ENSP00000420971.1:p.Val40Gly
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2054T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.103T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-233T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.322T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.*1T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.231T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.258T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2054T>G
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31080
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val40Gly
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: A
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum

5-75003668-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003668
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003668
    reference: chr 5
allele count: 5
allele frequency: 9.531798078389508e-5
allele num: 52456
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.176A>G
  hgvsp: ENSP00000425885.1:p.Ter59TrpextTer1
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.256A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.229A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.320A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-235A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-235A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2056A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.42A>G
  hgvsp: ENSP00000399481.2:p.Ile14Met
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.117A>G
  hgvsp: ENSP00000420971.1:p.Ile39Met
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.117A>G
  hgvsp: ENSP00000410216.2:p.Ile39Met
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-235A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.101A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2056A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30859
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13617
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter59TrpextTer1
num of homozygotes: 1
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

5-75003676-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003676
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003676
    reference: chr 5
allele count: 1
allele frequency: 1.834256575809824e-5
allele num: 54518
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2064T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.109T>C
  hgvsp: ENSP00000420971.1:p.Tyr37His
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-243T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.248T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.221T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-243T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.34T>C
  hgvsp: ENSP00000399481.2:p.Tyr12His
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.168T>C
  hgvsp: ENST00000515285.1:c.168T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.312T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.109T>C
  hgvsp: ENSP00000410216.2:p.Tyr37His
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-243T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.93T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2064T>C
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6043
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr37His
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

5-75003678-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003678
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003678
    reference: chr 5
allele count: 2
allele frequency: 2.442777927058651e-5
allele num: 81874
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.246A>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-245A>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.166A>T
  hgvsp: ENSP00000425885.1:p.Ile56Phe
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.91A>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2066A>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.107A>T
  hgvsp: ENSP00000420971.1:p.His36Leu
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-245A>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.107A>T
  hgvsp: ENSP00000410216.2:p.His36Leu
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2066A>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.32A>T
  hgvsp: ENSP00000399481.2:p.His11Leu
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.219A>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.310A>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-245A>T
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16003
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8880
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His36Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

5-75003678-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003678
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003678
    reference: chr 5
allele count: 45580
allele frequency: 5.567090895766665e-1
allele num: 81874
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-245A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.91A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.166A>G
  hgvsp: ENSP00000425885.1:p.Ile56Val
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.107A>G
  hgvsp: ENSP00000410216.2:p.His36Arg
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.32A>G
  hgvsp: ENSP00000399481.2:p.His11Arg
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-245A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2066A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.310A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.219A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-245A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2066A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.107A>G
  hgvsp: ENSP00000420971.1:p.His36Arg
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.246A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16003
  bin: 7.5e0
  variant carriers: 5740
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 5.25e1
  variant carriers: 656
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 445
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 9.75e1
  variant carriers: 2132
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.25e1
  variant carriers: 636
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.25e1
  variant carriers: 482
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 2.75e1
  variant carriers: 1774
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 2.5e0
  variant carriers: 403
genotype depth: GenotypeDepth
  all individuals: 13253
  bin: 1.25e1
  variant carriers: 11039
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 3.25e1
  variant carriers: 871
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.75e1
  variant carriers: 629
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 7972
  bin: 2.25e1
  variant carriers: 4148
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 169
genotype depth: GenotypeDepth
  all individuals: 8880
  bin: 1.75e1
  variant carriers: 8305
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 8.25e1
  variant carriers: 328
genotype quality: GenotypeQuality
hgvs: p.His36Arg
num of homozygotes: 11685
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

5-75003679-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003679
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003679
    reference: chr 5
allele count: 2
allele frequency: 3.100486776423899e-5
allele num: 64506
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-246C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.309C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.106C>T
  hgvsp: ENSP00000410216.2:p.His36Tyr
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-246C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2067C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.218C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.165C>T
  hgvsp: ENST00000515285.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-246C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.245C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.90C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.31C>T
  hgvsp: ENSP00000399481.2:p.His11Tyr
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.106C>T
  hgvsp: ENSP00000420971.1:p.His36Tyr
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2067C>T
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24766
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His36Tyr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

5-75003694-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003694
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003695
    reference: chr 5
allele count: 2
allele frequency: 3.233316088980859e-5
allele num: 61856
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-262dupA
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.149dupA
  hgvsp: ENSP00000425885.1:p.Asn50LysfsTer?
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2083dupA
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.202dupA
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.15dupA
  hgvsp: ENSP00000399481.2:p.Tyr6IlefsTer2
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.293dupA
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.90dupA
  hgvsp: ENSP00000420971.1:p.Tyr31IlefsTer2
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2083dupA
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-262dupA
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-262dupA
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.229dupA
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.90dupA
  hgvsp: ENSP00000410216.2:p.Tyr31IlefsTer2
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.74dupA
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12586
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr31IlefsTer2
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS

5-75003707-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003707
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003706
    reference: chr 5
allele count: 1
allele frequency: 1.689817161783095e-5
allele num: 59178
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.69-8delT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.10-8delT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.224-8delT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-267-8delT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.197-8delT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2096delT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-267-8delT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.85-8delT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.288-8delT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.144-8delT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.85-8delT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-8delT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2096delT
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.85-8delT
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: GA
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

5-75003714-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003714
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003714
    reference: chr 5
allele count: 32
allele frequency: 5.630630630630631e-4
allele num: 56832
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.288-14T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.10-14T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.85-14T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-267-14T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-267-14T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.197-14T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2102T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.69-14T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-14T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2102T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.224-14T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.144-14T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.85-14T>C
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14315
  bin: 1.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4460
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24730
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

5-75003715-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003715
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003715
    reference: chr 5
allele count: 4
allele frequency: 7.051440256672426e-5
allele num: 56726
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.85-15A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-267-15A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.85-15A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-267-15A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.224-15A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2103A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.197-15A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2103A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.10-15A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.288-15A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-15A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.144-15A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.69-15A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6815
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

5-75003725-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003725
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003725
    reference: chr 5
allele count: 2
allele frequency: 3.67498438131638e-5
allele num: 54422
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2113A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.10-25A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.144-25A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2113A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.197-25A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-267-25A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-267-25A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-25A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.224-25A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.85-25A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.69-25A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.288-25A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.85-25A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23988
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14522
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: T
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

5-75003725-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003725
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003725
    reference: chr 5
allele count: 3
allele frequency: 5.512476571974569e-5
allele num: 54422
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2113A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-25A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.69-25A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.85-25A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2113A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-267-25A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.197-25A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.85-25A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-267-25A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.10-25A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.288-25A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.224-25A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.144-25A>C
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14522
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23988
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

5-75003731-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003731
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003731
    reference: chr 5
allele count: 15
allele frequency: 2.886836027713626e-4
allele num: 51960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-267-31C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.69-31C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.197-31C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-267-31C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2119C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.10-31C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.85-31C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.144-31C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.224-31C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-31C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.85-31C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2119C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.288-31C>T
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10059
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23646
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14164
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

5-75003733-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003733
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003733
    reference: chr 5
allele count: 1
allele frequency: 1.973476476160404e-5
allele num: 50672
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.10-33T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2121T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.224-33T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.85-33T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-267-33T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2121T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.144-33T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-267-33T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-33T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.197-33T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.69-33T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.288-33T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.85-33T>C
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10521
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/5-75003741-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003741
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003741
    reference: chr 5
allele count: 1
allele frequency: 2.173724023997913e-5
allele num: 46004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-267-41G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-41G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.197-41G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2129G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.85-41G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.288-41G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-267-41G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.10-41G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.144-41G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.224-41G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.85-41G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.69-41G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2129G>T
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11691
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10957
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

5-75003743-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75003743
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75003743
    reference: chr 5
allele count: 3
allele frequency: 6.898454746136865e-5
allele num: 43488
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.85-43T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-128-2131T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-267-43T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.10-43T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.144-43T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.85-43T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-128-2131T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-267-43T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.197-43T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.288-43T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.224-43T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.69-43T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-43T>C
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10546
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3895
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11029
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26504
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

5-75008163-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008163
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008163
    reference: chr 5
allele count: 7
allele frequency: 5.79892637020346e-5
allele num: 120712
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4463T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+516T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.9+38T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+516T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.68+20T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-268+42T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+269T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+516T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+516T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+269T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4968T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+516T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+269T>C
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5639
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5370
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6793
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

5-75008176-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008176
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008176
    reference: chr 5
allele count: 2
allele frequency: 1.656397005234214e-5
allele num: 120744
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+256T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.9+25T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+256T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.68+7T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+503T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4955T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+503T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+503T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+503T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-268+29T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+503T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+256T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4476T>A
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5639
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5829
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.68+7T>A
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/5-75008183-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008183
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008183
    reference: chr 5
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+249G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+496G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4948G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+249G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.68G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.9+18G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+496G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+496G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-268+22G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4483G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+249G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+496G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+496G>T
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5639
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.68G>T
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

5-75008190-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008190
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008190
    reference: chr 5
allele count: 2
allele frequency: 1.656204971927326e-5
allele num: 120758
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+242T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+489T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4941T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+242T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+489T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+489T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+489T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+489T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.61T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4490T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+242T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.9+11T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-268+15T>C
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5829
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5639
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6795
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

5-75008193-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008193
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008193
    reference: chr 5
allele count: 34782
allele frequency: 2.880735464634752e-1
allele num: 120740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.9+8A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+239A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-268+12A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+486A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+239A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+486A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4938A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4493A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+486A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.58A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+239A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+486A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+486A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 2.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 8.25e1
  variant carriers: 1134
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 5.75e1
  variant carriers: 339
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 3.75e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 3.25e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 9.25e1
  variant carriers: 1514
genotype depth: GenotypeDepth
  all individuals: 25295
  bin: 9.75e1
  variant carriers: 21464
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 5.25e1
  variant carriers: 229
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 4.25e1
  variant carriers: 166
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 6.75e1
  variant carriers: 654
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 2.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 7.25e1
  variant carriers: 827
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 7.75e1
  variant carriers: 1028
genotype quality: GenotypeQuality
hgvs: c.9+8A>G
num of homozygotes: 5173
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/5-75008201-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008201
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008201
    reference: chr 5
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+478G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.9G>T
  hgvsp: ENSP00000399481.2:p.Trp3Cys
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+478G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-268+4G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+478G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.50G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+231G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+478G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4501G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4930G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+231G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+478G>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+231G>T
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12196
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4961
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp3Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

5-75008204-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008204
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008204
    reference: chr 5
allele count: 2
allele frequency: 1.656204971927326e-5
allele num: 120758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4504G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+228G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.47G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4927G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+475G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+228G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.6G>A
  hgvsp: ENST00000446329.2:c.6G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+475G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-268+1G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+475G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+475G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+475G>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+228G>A
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.-268+1G>A
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

5-75008209-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008209
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008209
    reference: chr 5
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.42A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4509A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+470A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.1A>C
  hgvsp: ENSP00000399481.2:p.Met1?
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-272A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+470A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+470A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+470A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+470A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+223A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+223A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+223A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4922A>C
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4961
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD

5-75008216-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008216
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008216
    reference: chr 5
allele count: 9
allele frequency: 7.452922373672965e-5
allele num: 120758
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+216A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+216A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+463A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.-7A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.35A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+463A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-279A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4516A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+463A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+216A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+463A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+463A>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4915A>C
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4961
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5012
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

5-75008222-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008222
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008222
    reference: chr 5
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+457A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+457A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.29A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+210A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+457A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+457A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-285A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+457A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4909A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.-13A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4522A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+210A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+210A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4670
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5012
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12191
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4961
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

5-75008223-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008223
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008223
    reference: chr 5
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+209C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+209C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.-14C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4523C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.28C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-286C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+209C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+456C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4908C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+456C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+456C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+456C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+456C>T
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4961
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4670
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum

5-75008232-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008232
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008232
    reference: chr 5
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+447G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.-23G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+447G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+200G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+447G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4532G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.19G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4899G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+447G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+447G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-295G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+200G>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+200G>C
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5012
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12191
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4961
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

5-75008247-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008247
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008247
    reference: chr 5
allele count: 148
allele frequency: 1.22557138125207e-3
allele num: 120760
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+432A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+185A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-310A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+432A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000504862
  gene symbol: POC5
  hgvsc: ENST00000504862.1:n.4A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+432A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4547A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.-38A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+185A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+432A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4884A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+185A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+432A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 7.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 8.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 5004
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2904
  bin: 9.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4964
  bin: 7.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
num of homozygotes: 2
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

5-75008256-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008256
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008256
    reference: chr 5
allele count: 3
allele frequency: 2.484348603796085e-5
allele num: 120756
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+423A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4556A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+176A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+176A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4875A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+423A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+423A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+423A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000426796
  ensembl transcript: ENST00000510798
  gene symbol: POC5
  hgvsc: ENST00000510798.1:c.-319A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000399481
  ensembl transcript: ENST00000446329
  gene symbol: POC5
  hgvsc: ENST00000446329.2:c.-47A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+176A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+423A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4176
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5011
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12192
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4652
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4675
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ

5-75008388-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008388
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008388
    reference: chr 5
allele count: 1
allele frequency: 3.509510774198076e-5
allele num: 28494
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+291T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+44T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+291T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+291T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4688T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+44T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+291T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+44T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+291T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4743T>C
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13950
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/5-75008389-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008389
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008389
    reference: chr 5
allele count: 1
allele frequency: 3.503117774819589e-5
allele num: 28546
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+290T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+290T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4742T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+290T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+43T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+43T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+43T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+290T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+290T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4689T>G
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5314
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15165
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/5-75008393-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008393
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008393
    reference: chr 5
allele count: 1
allele frequency: 4.035838243603196e-5
allele num: 24778
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+39T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+39T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+286T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+286T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+286T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4738T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+286T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4693T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+39T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+286T>G
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12882
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5391
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29384
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

5-75008400-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008400
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008400
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 21914
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+279T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+32T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+279T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4731T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+279T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+32T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+32T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+279T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+279T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4700T>C
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11055
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4052
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32469
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/5-75008401-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008401
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008402
    reference: chr 5
allele count: 3
allele frequency: 1.427076396156408e-4
allele num: 21022
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+277dupT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+277dupT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4729dupT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4702dupT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+30dupT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+30dupT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+277dupT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+30dupT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+277dupT
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+277dupT
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10615
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31585
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1833
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32642
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

5-75008402-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008402
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008402
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 20608
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+277T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+30T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+277T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+30T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+277T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+30T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-267-4702T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+277T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+277T>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4729T>A
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 31871
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10163
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum

5-75008424-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008424
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008424
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 14476
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+255A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+255A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-268+4707A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+255A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+255A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.196+8A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+255A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.287+8A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4707A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.143+8A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29597
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2595
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
hgvs: n.287+8A>G
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

5-75008447-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008447
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008447
    reference: chr 5
allele count: 2
allele frequency: 1.568381430363864e-4
allele num: 12752
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+232A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.128A>G
  hgvsp: ENSP00000425885.1:p.Asn43Ser
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+232A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4684A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+232A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.272A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.181A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+232A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-268+4684A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+232A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22916
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asn43Ser
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

5-75008459-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008459
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008459
    reference: chr 5
allele count: 44
allele frequency: 3.694374475230898e-3
allele num: 11910
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+220A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-268+4672A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4672A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.260A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+220A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.116A>G
  hgvsp: ENSP00000425885.1:p.Tyr39Cys
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.169A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+220A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+220A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+220A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20055
  bin: 2.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 7.5e0
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 9.75e1
  variant carriers: 47
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 8.75e1
  variant carriers: 1
hgvs: p.Tyr39Cys
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP

5-75008477-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008477
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008477
    reference: chr 5
allele count: 7
allele frequency: 6.759366550791811e-4
allele num: 10356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.98A>G
  hgvsp: ENSP00000425885.1:p.Asn33Ser
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+202A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-268+4654A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+202A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+202A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4654A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.242A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.151A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+202A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+202A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15704
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2574
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn33Ser
num of homozygotes: 1
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

5-75008484-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008484
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008484
    reference: chr 5
allele count: 1
allele frequency: 1.006238679814852e-4
allele num: 9938
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+195T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+195T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.144T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+195T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.91T>C
  hgvsp: ENST00000515285.1:c.91T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4647T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+195T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.235T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+195T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-268+4647T>C
  variant of: http://identifiers.org/hgnc/26658
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14959
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 880
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4123
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu31Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

5-75008508-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008508
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008508
    reference: chr 5
allele count: 3
allele frequency: 3.565486094604231e-4
allele num: 8414
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-268+4623A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.138-18A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.229-18A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+171A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+171A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+171A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4623A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+171A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.85-18A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+171A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14842
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4080
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

5-75008509-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008509
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008509
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 8264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.85-19C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-268+4622C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+170C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+170C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+170C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.229-19C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+170C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.138-19C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+170C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4622C>T
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14924
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

5-75008528-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008528
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008528
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 7596
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+151C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-268+4603C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+151C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.138-38C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+151C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.85-38C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+151C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+151C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4603C>T
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.229-38C>T
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17401
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: G
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

5-75008633-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008633
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008633
    reference: chr 5
allele count: 1
allele frequency: 2.390857361449816e-5
allele num: 41826
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-268+4498C>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+46C>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.84+46C>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+46C>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+46C>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+46C>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4498C>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.137+46C>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+46C>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.228+46C>G
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1120
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/5-75008643-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008643
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008643
    reference: chr 5
allele count: 1
allele frequency: 2.335575485799701e-5
allele num: 42816
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+36T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+36T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-268+4488T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+36T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4488T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.228+36T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.137+36T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.84+36T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+36T>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+36T>G
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9762
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

5-75008646-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008646
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008646
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 43712
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4485T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.137+33T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+33T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.84+33T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+33T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+33T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+33T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.228+33T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-268+4485T>C
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+33T>C
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29622
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8536
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9073
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

5-75008648-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008648
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008647
    reference: chr 5
allele count: 2
allele frequency: 4.531242919932937e-5
allele num: 44138
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.228+30delC
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+30delC
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+30delC
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+30delC
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.84+30delC
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4482delC
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.137+30delC
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+30delC
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-268+4482delC
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+30delC
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 7678
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8946
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3790
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26509
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6435
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
reference allele: AG
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

5-75008649-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008649
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008649
    reference: chr 5
allele count: 1
allele frequency: 2.255808707421611e-5
allele num: 44330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+30C>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+30C>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-268+4482C>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.84+30C>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.228+30C>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+30C>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+30C>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.137+30C>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+30C>A
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4482C>A
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7289
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8878
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3992
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3759
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

5-75008653-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008653
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008653
    reference: chr 5
allele count: 1
allele frequency: 2.16132099939483e-5
allele num: 46268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+26A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.84+26A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-268+4478A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+26A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+26A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+26A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+26A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4478A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.137+26A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.228+26A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5521
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31385
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1567
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2666
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6763
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

5-75008667-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008667
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008666
    reference: chr 5
allele count: 6
allele frequency: 1.058387722702417e-4
allele num: 56690
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.84+11delA
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+11delA
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+11delA
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-268+4463delA
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4463delA
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.137+11delA
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+11delA
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.228+11delA
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+11delA
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+11delA
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29790
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13223
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6313
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2605
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1809
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: AT
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

5-75008668-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75008668
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 75008668
    reference: chr 5
allele count: 2
allele frequency: 3.468248187840322e-5
allele num: 57666
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425726
  ensembl transcript: ENST00000502826
  gene symbol: POC5
  hgvsc: ENST00000502826.1:c.-129+4463A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000508467
  gene symbol: POC5
  hgvsc: ENST00000508467.1:n.223+11A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000420971
  ensembl transcript: ENST00000514838
  gene symbol: POC5
  hgvsc: ENST00000514838.2:c.84+11A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000424264
  ensembl transcript: ENST00000503835
  gene symbol: POC5
  hgvsc: ENST00000503835.1:c.-268+4463A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425108
  ensembl transcript: ENST00000506164
  gene symbol: POC5
  hgvsc: ENST00000506164.1:c.-129+11A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000410216
  ensembl transcript: ENST00000428202
  gene symbol: POC5
  hgvsc: ENST00000428202.2:c.84+11A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000512125
  gene symbol: POC5
  hgvsc: ENST00000512125.1:n.228+11A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000425885
  ensembl transcript: ENST00000515285
  gene symbol: POC5
  hgvsc: ENST00000515285.1:c.84+11A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl transcript: ENST00000507421
  gene symbol: POC5
  hgvsc: ENST00000507421.1:n.137+11A>G
  variant of: http://identifiers.org/hgnc/26658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000152359
  ensembl protein: ENSP00000369842
  ensembl transcript: ENST00000380475
  gene symbol: POC5
  hgvsc: ENST00000380475.2:c.-268+11A>G
  variant of: http://identifiers.org/hgnc/26658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6151
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13781
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
reference allele: T

GenotypeDepth
all individuals: 14
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 123
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3258
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3698
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4576
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 282
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28249
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1884
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 230
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8160
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6968
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.43e-2

QD
type: SiteQuality
SIO_000300: 2.741e1

VQSLOD
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.52604e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 37
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1169
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 193
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5081
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30626
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2856
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3877
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 308
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1936
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7194
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8342
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1632
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.72021e5

QD
type: SiteQuality
SIO_000300: 9.300000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.340000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeDepth
all individuals: 21
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 72
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1326
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9352
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 32598
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1115
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1037
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6356
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7768
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2170
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 240
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.347e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.270000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.137e1

DP
type: SiteQuality
SIO_000300: 4.44049e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeDepth
all individuals: 442
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 723
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 36
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6735
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1093
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27713
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1041
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 624
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16450
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1352
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 1
allele frequency: 1.265502404454569e-4
allele num: 7902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1658
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 488
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10140
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

DP
type: SiteQuality
SIO_000300: 5.00003e5

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.239e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.05e-2

GenotypeDepth
all individuals: 259
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 150
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20476
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1121
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1608
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23474
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1356
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 369
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7214
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 2
allele frequency: 7.462686567164179e-3
allele num: 268
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2534
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1734
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7980
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.892e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.79e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

DP
type: SiteQuality
SIO_000300: 5.57973e5

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.26e0

QD
type: SiteQuality
SIO_000300: 1.161e1

FS
type: SiteQuality
SIO_000300: 1.714e0

GenotypeDepth
all individuals: 124
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 197
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 71
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18109
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25000
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7353
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2174
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1356
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2640
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 648
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8024
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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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

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

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

InbreedingCoeff
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MQ
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FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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QD
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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African
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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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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 17512
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2304
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 1.114454474534715e-4
allele num: 17946
num of homozygotes: 1

FS
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SIO_000300: 6.368e0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 3756
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 18678
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 4.184100418410042e-4
allele num: 2390
num of homozygotes: 0

South Asian
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allele count: 0
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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

BaseQRankSum
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SIO_000300: 1.07e0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 2.513826043237808e-4
allele num: 3978
num of homozygotes: 0

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

Latino
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Other
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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DP
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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QD
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ClippingRankSum
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VQSLOD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 23362
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 257
bin: 9.25e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 3.912363067292645e-4
allele num: 2556
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.149613069647464e-4
allele num: 4652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2910
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9116
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.648804616652927e-4
allele num: 24260
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3202
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

QD
type: SiteQuality
SIO_000300: 1.14e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.299999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

FS
type: SiteQuality
SIO_000300: 2.222e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.73047e5

GenotypeDepth
all individuals: 45
bin: 7.25e1
variant carriers: 8

GenotypeDepth
all individuals: 85
bin: 9.75e1
variant carriers: 12

GenotypeDepth
all individuals: 18
bin: 9.25e1
variant carriers: 4

GenotypeDepth
all individuals: 134
bin: 5.25e1
variant carriers: 10

GenotypeQuality
all individuals: 475
bin: 5.25e1
variant carriers: 6

GenotypeQuality
all individuals: 3582
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1412
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 264
bin: 9.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1488
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 895
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 179
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 12269
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 996
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30882
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 600
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1786
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 212
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 567
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1628
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 156
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1558
bin: 9.75e1
variant carriers: 195

GenotypeQuality
all individuals: 448
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 455
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 133
allele frequency: 1.431030772541425e-2
allele num: 9294
num of homozygotes: 4

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3438
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 3.311258278145695e-4
allele num: 3020
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.347417840375587e-3
allele num: 426
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 6.213753106876554e-4
allele num: 4828
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 7.147962830593281e-4
allele num: 2798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 74
allele frequency: 2.889045053486374e-3
allele num: 25614
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.194e1

DP
type: SiteQuality
SIO_000300: 7.93878e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

GenotypeDepth
all individuals: 1992
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 264
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1668
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3410
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30416
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1087
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1842
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12273
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.810685161191982e-5
allele num: 26242
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4918
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3096
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2934
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.399999999999999e-3

QD
type: SiteQuality
SIO_000300: 1.09e1

FS
type: SiteQuality
SIO_000300: 1.1167e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.29e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.363e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

DP
type: SiteQuality
SIO_000300: 7.98686e5

GenotypeDepth
all individuals: 76
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1787
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3188
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1903
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 933
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12308
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 385
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1718
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1474
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29939
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1407
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1114
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3172
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3112
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26990
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 2.730748225013654e-4
allele num: 3662
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.416e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.0e-1

DP
type: SiteQuality
SIO_000300: 8.07976e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

FS
type: SiteQuality
SIO_000300: 6.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.29e-1

GenotypeDepth
all individuals: 461
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 266
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 14
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1919
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29683
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 7.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 865
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1842
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1725
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 475
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1489
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12346
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27284
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3174
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 9.819324430479183e-4
allele num: 5092
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3220
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.12657e5

VQSLOD
type: SiteQuality
SIO_000300: -5.619e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.09e-1

FS
type: SiteQuality
SIO_000300: 1.5199e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.01e-1

QD
type: SiteQuality
SIO_000300: 1.716e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 78
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 14
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 880
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29192
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1412
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1952
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2815
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1220
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12580
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1781
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1541
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2020
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.515927149989452e-5
allele num: 28442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3310
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5250
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3940
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 462
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.469e0

DP
type: SiteQuality
SIO_000300: 8.28033e5

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.62e-1

QD
type: SiteQuality
SIO_000300: 1.378e1

GenotypeDepth
all individuals: 693
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 659
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 332
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 212
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1940
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4775
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1368
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2255
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10910
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1714
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1566
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1177
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1431
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24221
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 806
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8004
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.628986714808128e-5
allele num: 43206
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-1

DP
type: SiteQuality
SIO_000300: 1.478131e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.055e-1

QD
type: SiteQuality
SIO_000300: 1.97e1

VQSLOD
type: SiteQuality
SIO_000300: 6.02e0

GenotypeDepth
all individuals: 670
bin: 6.75e1
variant carriers: 638

GenotypeDepth
all individuals: 732
bin: 5.75e1
variant carriers: 706

GenotypeDepth
all individuals: 765
bin: 3.75e1
variant carriers: 641

GenotypeDepth
all individuals: 734
bin: 4.25e1
variant carriers: 648

GenotypeQuality
all individuals: 1045
bin: 6.75e1
variant carriers: 769

GenotypeQuality
all individuals: 24221
bin: 9.75e1
variant carriers: 23809

GenotypeQuality
all individuals: 806
bin: 8.75e1
variant carriers: 777

GenotypeQuality
all individuals: 4775
bin: 6.25e1
variant carriers: 1007

GenotypeQuality
all individuals: 628
bin: 1.25e1
variant carriers: 378

GenotypeQuality
all individuals: 10910
bin: 2.25e1
variant carriers: 1346

GenotypeQuality
all individuals: 905
bin: 9.25e1
variant carriers: 854

GenotypeQuality
all individuals: 1177
bin: 2.75e1
variant carriers: 800

GenotypeQuality
all individuals: 1431
bin: 5.25e1
variant carriers: 1273

GenotypeQuality
all individuals: 1566
bin: 4.75e1
variant carriers: 1448

GenotypeQuality
all individuals: 2255
bin: 2.5e0
variant carriers: 173

GenotypeQuality
all individuals: 918
bin: 4.25e1
variant carriers: 840

GenotypeQuality
all individuals: 1422
bin: 7.5e0
variant carriers: 318

GenotypeQuality
all individuals: 876
bin: 5.75e1
variant carriers: 781

GenotypeQuality
all individuals: 1368
bin: 1.75e1
variant carriers: 927

GenotypeQuality
all individuals: 781
bin: 7.75e1
variant carriers: 688

GenotypeQuality
all individuals: 1714
bin: 3.75e1
variant carriers: 1566

GenotypeQuality
all individuals: 833
bin: 8.25e1
variant carriers: 754

GenotypeQuality
all individuals: 1940
bin: 3.25e1
variant carriers: 1626

GenotypeQuality
all individuals: 542
bin: 7.25e1
variant carriers: 463

African
type: Population
allele count: 6970
allele frequency: 8.708145927036481e-1
allele num: 8004
num of homozygotes: 3020

Latino
type: Population
allele count: 3410
allele frequency: 5.202929508696978e-1
allele num: 6554
num of homozygotes: 662

European (Non-Finnish)
type: Population
allele count: 21164
allele frequency: 4.898393741609962e-1
allele num: 43206
num of homozygotes: 4180

European (Finnish)
type: Population
allele count: 2298
allele frequency: 4.937688010313709e-1
allele num: 4654
num of homozygotes: 492

Other
type: Population
allele count: 352
allele frequency: 5.317220543806647e-1
allele num: 662
num of homozygotes: 84

South Asian
type: Population
allele count: 7417
allele frequency: 6.006640751538711e-1
allele num: 12348
num of homozygotes: 2157

East Asian
type: Population
allele count: 3969
allele frequency: 6.15730685696556e-1
allele num: 6446
num of homozygotes: 1090

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.055e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

DP
type: SiteQuality
SIO_000300: 1.478131e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e-1

QD
type: SiteQuality
SIO_000300: 1.97e1

GenotypeDepth
all individuals: 11644
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5243
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1038
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 95
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1979
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variant carriers: 0

GenotypeQuality
all individuals: 1829
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3019
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variant carriers: 0

GenotypeQuality
all individuals: 970
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 737
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variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29588
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2183
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1890
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variant carriers: 0

GenotypeQuality
all individuals: 739
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variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 498
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variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
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GenotypeQuality
all individuals: 119
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variant carriers: 0

GenotypeQuality
all individuals: 2508
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 594
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11633
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.889628364450203e-5
allele num: 33958
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10426
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 526
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.709e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

QD
type: SiteQuality
SIO_000300: 1.126e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.203e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.025609e6

VQSLOD
type: SiteQuality
SIO_000300: 5.22e-1

GenotypeDepth
all individuals: 110
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 95
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variant carriers: 0

GenotypeDepth
all individuals: 68
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variant carriers: 0

GenotypeDepth
all individuals: 7070
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variant carriers: 0

GenotypeQuality
all individuals: 1531
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
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variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
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variant carriers: 0

GenotypeQuality
all individuals: 3972
bin: 7.5e0
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GenotypeQuality
all individuals: 1615
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2230
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
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variant carriers: 0

GenotypeQuality
all individuals: 31330
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variant carriers: 0

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

GenotypeQuality
all individuals: 272
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1918
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10448
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
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variant carriers: 0

GenotypeQuality
all individuals: 2496
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 196
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.97199763360284e-4
allele num: 10142
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5978
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3668
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.516e1

DP
type: SiteQuality
SIO_000300: 9.892e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

FS
type: SiteQuality
SIO_000300: 6.368e0

GenotypeDepth
all individuals: 5601
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 537
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
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variant carriers: 0

GenotypeDepth
all individuals: 60
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variant carriers: 0

GenotypeDepth
all individuals: 95
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variant carriers: 0

GenotypeQuality
all individuals: 1966
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variant carriers: 0

GenotypeQuality
all individuals: 5448
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 399
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variant carriers: 0

GenotypeQuality
all individuals: 8955
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variant carriers: 0

GenotypeQuality
all individuals: 1465
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variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2493
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variant carriers: 1

GenotypeQuality
all individuals: 194
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variant carriers: 0

GenotypeQuality
all individuals: 108
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variant carriers: 0

GenotypeQuality
all individuals: 227
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variant carriers: 0

GenotypeQuality
all individuals: 2351
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variant carriers: 0

GenotypeQuality
all individuals: 298
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variant carriers: 0

GenotypeQuality
all individuals: 1372
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
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GenotypeQuality
all individuals: 32095
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variant carriers: 0

GenotypeQuality
all individuals: 1017
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 413
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variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.012145748987854e-4
allele num: 9880
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4080
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31024
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4412
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.725e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.091e0

QD
type: SiteQuality
SIO_000300: 2.389e1

MQ
type: SiteQuality
SIO_000300: 6.049e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.18e-2

DP
type: SiteQuality
SIO_000300: 9.50083e5

VQSLOD
type: SiteQuality
SIO_000300: 3.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

GenotypeDepth
all individuals: 111
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1397
bin: 1.75e1
variant carriers: 5

GenotypeDepth
all individuals: 166
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7059
bin: 7.5e0
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GenotypeQuality
all individuals: 1377
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1844
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2513
bin: 9.75e1
variant carriers: 30

GenotypeQuality
all individuals: 357
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 176
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2482
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2082
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 8.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 274
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variant carriers: 0

GenotypeQuality
all individuals: 7379
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 207
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 374
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 31114
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 739
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9640
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 5.417118093174431e-4
allele num: 5538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 25
allele frequency: 8.410711882653747e-4
allele num: 29724
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 1.046572475143904e-3
allele num: 3822
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3470
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.59e-1

FS
type: SiteQuality
SIO_000300: 6.37e-1

QD
type: SiteQuality
SIO_000300: 1.258e1

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.43e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 9.14938e5

BaseQRankSum
type: SiteQuality
SIO_000300: 7.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

GenotypeDepth
all individuals: 24764
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 245
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
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GenotypeQuality
all individuals: 31281
bin: 2.25e1
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GenotypeQuality
all individuals: 1223
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variant carriers: 0

GenotypeQuality
all individuals: 106
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GenotypeQuality
all individuals: 1385
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
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GenotypeQuality
all individuals: 7083
bin: 7.5e0
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GenotypeQuality
all individuals: 271
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2480
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
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GenotypeQuality
all individuals: 7458
bin: 6.25e1
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GenotypeQuality
all individuals: 2072
bin: 3.25e1
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GenotypeQuality
all individuals: 352
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GenotypeQuality
all individuals: 166
bin: 5.75e1
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GenotypeQuality
all individuals: 374
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1719
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2488
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 190
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3466
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 4.146796599626788e-4
allele num: 9646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3812
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29652
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.43e-2

QD
type: SiteQuality
SIO_000300: 1.513e1

VQSLOD
type: SiteQuality
SIO_000300: 6.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

FS
type: SiteQuality
SIO_000300: 3.342e0

MQRankSum
type: SiteQuality
SIO_000300: 4.61e-1

DP
type: SiteQuality
SIO_000300: 9.14357e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-2

GenotypeDepth
all individuals: 95
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 64
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variant carriers: 0

GenotypeDepth
all individuals: 1040
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 201
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GenotypeQuality
all individuals: 315
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GenotypeQuality
all individuals: 311
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GenotypeQuality
all individuals: 1703
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variant carriers: 0

GenotypeQuality
all individuals: 188
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GenotypeQuality
all individuals: 97
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GenotypeQuality
all individuals: 5973
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GenotypeQuality
all individuals: 2103
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GenotypeQuality
all individuals: 2612
bin: 2.75e1
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GenotypeQuality
all individuals: 927
bin: 3.75e1
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GenotypeQuality
all individuals: 9326
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GenotypeQuality
all individuals: 2397
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GenotypeQuality
all individuals: 105
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GenotypeQuality
all individuals: 175
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GenotypeQuality
all individuals: 115
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GenotypeQuality
all individuals: 2488
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GenotypeQuality
all individuals: 1047
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3382
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5306
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 436
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 5.605381165919282e-4
allele num: 3568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3950
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.75706e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.66e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.84e-1

QD
type: SiteQuality
SIO_000300: 1.285e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.52e-2

ClippingRankSum
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2488
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variant carriers: 2

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 436
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3382
num of homozygotes: 0

African
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allele count: 3
allele frequency: 5.653976630229929e-4
allele num: 5306
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 count: 0
allele frequency: 0.0e0
allele num: 9388
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 28392
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.66e0

MQRankSum
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MQ
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DP
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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SIO_000300: 0.0e0

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -7.84e-1

GenotypeDepth
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variant carriers: 1

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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variant carriers: 15

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3252
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5088
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3282
num of homozygotes: 0

South Asian
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allele count: 9
allele frequency: 9.806057964698192e-4
allele num: 9178
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 27066
num of homozygotes: 0

East Asian
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allele count: 6
allele frequency: 1.634877384196185e-3
allele num: 3670
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.52e-1

FS
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QD
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MQ
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: -2.08e-2

MQRankSum
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VQSLOD
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DP
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SIO_000300: 8.44427e5

GenotypeDepth
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variant carriers: 0

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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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3152
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

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

South Asian
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allele frequency: 1.105705440070765e-4
allele num: 9044
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3208
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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e0

MQRankSum
type: SiteQuality
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InbreedingCoeff
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DP
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 5.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.73e-1

GenotypeDepth
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variant carriers: 0

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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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3032
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23640
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2726
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4552
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3022
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.72e-1

DP
type: SiteQuality
SIO_000300: 7.94676e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.64e0

QD
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MQ
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VQSLOD
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BaseQRankSum
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FS
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SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.58e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.37e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 1

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2714
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
type: Population
allele count: 1
allele frequency: 3.422313483915127e-4
allele num: 2922
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 8.99199712256092e-5
allele num: 22242
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2452
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
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MQ
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DP
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InbreedingCoeff
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BaseQRankSum
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FS
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VQSLOD
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
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SIO_000300: 1.439e1

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.047777441790142e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.497751124437781e-5
allele num: 66700
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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QD
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GenotypeDepth
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variant carriers: 2

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

Latino
type: Population
allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66726
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

South Asian
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African
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allele count: 0
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MQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

VQSLOD
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QD
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BaseQRankSum
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SIO_000300: 2.66e0

DP
type: SiteQuality
SIO_000300: 4.08856e6

MQ
type: SiteQuality
SIO_000300: 5.982e1

FS
type: SiteQuality
SIO_000300: 1.977e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

GenotypeDepth
all individuals: 6795
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5830
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variant carriers: 1

GenotypeDepth
all individuals: 2004
bin: 9.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56581
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 0
bin: 1.25e1
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GenotypeQuality
all individuals: 513
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.308e0

DP
type: SiteQuality
SIO_000300: 4.088849e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.88e-1

QD
type: SiteQuality
SIO_000300: 8.550000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.69e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.028e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.2e-1

GenotypeDepth
all individuals: 5374
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variant carriers: 1

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeDepth
all individuals: 2004
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variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 680
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GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 326
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GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56581
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 430
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variant carriers: 0

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

GenotypeQuality
all individuals: 822
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.946e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e0

FS
type: SiteQuality
SIO_000300: 7.169e0

QD
type: SiteQuality
SIO_000300: 1.121e1

DP
type: SiteQuality
SIO_000300: 4.089034e6

VQSLOD
type: SiteQuality
SIO_000300: 3.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.27e-1

GenotypeDepth
all individuals: 3353
bin: 6.25e1
variant carriers: 470

GenotypeDepth
all individuals: 2872
bin: 8.75e1
variant carriers: 1353

GenotypeDepth
all individuals: 3
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2392
bin: 4.75e1
variant carriers: 174

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 245
bin: 8.25e1
variant carriers: 7

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

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 11
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variant carriers: 0

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

GenotypeQuality
all individuals: 8
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variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 182
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variant carriers: 2

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 355
bin: 9.25e1
variant carriers: 7

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 149
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variant carriers: 4

GenotypeQuality
all individuals: 313
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variant carriers: 3

GenotypeQuality
all individuals: 231
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variant carriers: 4

GenotypeQuality
all individuals: 58659
bin: 9.75e1
variant carriers: 29570

African
type: Population
allele count: 3393
allele frequency: 3.462244897959184e-1
allele num: 9800
num of homozygotes: 590

East Asian
type: Population
allele count: 1644
allele frequency: 1.907635182176839e-1
allele num: 8618
num of homozygotes: 143

Latino
type: Population
allele count: 2814
allele frequency: 2.432152117545376e-1
allele num: 11570
num of homozygotes: 349

South Asian
type: Population
allele count: 5457
allele frequency: 3.30526953361599e-1
allele num: 16510
num of homozygotes: 931

European (Finnish)
type: Population
allele count: 2131
allele frequency: 3.224878934624698e-1
allele num: 6608
num of homozygotes: 367

European (Non-Finnish)
type: Population
allele count: 19089
allele frequency: 2.860375209781827e-1
allele num: 66736
num of homozygotes: 2760

Other
type: Population
allele count: 254
allele frequency: 2.828507795100223e-1
allele num: 898
num of homozygotes: 33

MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.15e-1

QD
type: SiteQuality
SIO_000300: 1.727e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.45e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.32e0

DP
type: SiteQuality
SIO_000300: 5.767413e6

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

GenotypeDepth
all individuals: 5013
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3598
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5181
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
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variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 620
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variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 57770
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 204
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 6.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.798e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e0

FS
type: SiteQuality
SIO_000300: 5.038e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.157e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -8.99e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.33e0

QD
type: SiteQuality
SIO_000300: 9.949999999999999e0

DP
type: SiteQuality
SIO_000300: 4.658866e6

GenotypeDepth
all individuals: 12195
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4082
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variant carriers: 0

GenotypeDepth
all individuals: 5180
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variant carriers: 0

GenotypeDepth
all individuals: 3598
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variant carriers: 0

GenotypeQuality
all individuals: 57770
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variant carriers: 2

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 399
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 204
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variant carriers: 0

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

GenotypeQuality
all individuals: 430
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 292
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variant carriers: 0

GenotypeQuality
all individuals: 337
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GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 620
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GenotypeQuality
all individuals: 315
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.040816326530612e-4
allele num: 9800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.73e0

QD
type: SiteQuality
SIO_000300: 1.237e1

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.77e-1

FS
type: SiteQuality
SIO_000300: 8.244999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.569e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.65884e6

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

GenotypeDepth
all individuals: 5013
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4176
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variant carriers: 0

GenotypeDepth
all individuals: 12194
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variant carriers: 1

GenotypeDepth
all individuals: 3278
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 0
bin: 2.5e0
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GenotypeQuality
all individuals: 315
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 620
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GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 339
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GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 292
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GenotypeQuality
all individuals: 431
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 203
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GenotypeQuality
all individuals: 394
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 4.658834e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e0

FS
type: SiteQuality
SIO_000300: 1.364e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQRankSum
type: SiteQuality
SIO_000300: -1.023e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.13e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.117e0

QD
type: SiteQuality
SIO_000300: 1.826e1

GenotypeDepth
all individuals: 2379
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variant carriers: 0

GenotypeDepth
all individuals: 2893
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GenotypeDepth
all individuals: 12194
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57771
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 430
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GenotypeQuality
all individuals: 620
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GenotypeQuality
all individuals: 204
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 398
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GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 291
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GenotypeQuality
all individuals: 336
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GenotypeQuality
all individuals: 315
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 9.183673469387755e-4
allele num: 9800
num of homozygotes: 0

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

East Asian
type: Population
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allele frequency: 0.0e0
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South Asian
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European (Finnish)
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VQSLOD
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MQRankSum
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ClippingRankSum
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FS
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QD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

East Asian
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European (Non-Finnish)
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South Asian
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Other
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Latino
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African
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VQSLOD
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DP
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BaseQRankSum
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MQ
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QD
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InbreedingCoeff
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FS
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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East Asian
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European (Non-Finnish)
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South Asian
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Other
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European (Finnish)
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BaseQRankSum
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MQ
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QD
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ClippingRankSum
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VQSLOD
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FS
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MQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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European (Non-Finnish)
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East Asian
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Other
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South Asian
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Latino
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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ReadPosRankSum
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FS
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VQSLOD
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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Other
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European (Non-Finnish)
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Latino
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South Asian
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MQRankSum
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MQ
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InbreedingCoeff
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QD
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ClippingRankSum
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ReadPosRankSum
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FS
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VQSLOD
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BaseQRankSum
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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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European (Non-Finnish)
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East Asian
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South Asian
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African
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European (Finnish)
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Latino
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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SIO_000300: 1.69e0

FS
type: SiteQuality
SIO_000300: 2.862e0

QD
type: SiteQuality
SIO_000300: 1.587e1

VQSLOD
type: SiteQuality
SIO_000300: -3.535e0

DP
type: SiteQuality
SIO_000300: 4.58333e5

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

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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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: 5.75e1
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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1096
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1772
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1010
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 9.109127345600292e-5
allele num: 10978
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8814
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.26985e5

MQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

QD
type: SiteQuality
SIO_000300: 8.23e0

MQ
type: SiteQuality
SIO_000300: 5.609e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.419999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.23e-1

GenotypeQuality
all individuals: 1375
bin: 2.5e0
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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bin: 8.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9418
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.522e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.93e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.219e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.94631e5

VQSLOD
type: SiteQuality
SIO_000300: -3.681e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

QD
type: SiteQuality
SIO_000300: 1.164e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.22e0

GenotypeQuality
all individuals: 58
bin: 4.75e1
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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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.569728700618753e-4
allele num: 8404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1440
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.19e-1

DP
type: SiteQuality
SIO_000300: 3.87537e5

FS
type: SiteQuality
SIO_000300: 6.513e0

MQRankSum
type: SiteQuality
SIO_000300: 4.75e-1

QD
type: SiteQuality
SIO_000300: 8.359999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.28e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.03e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.474e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.3e-1

MQ
type: SiteQuality
SIO_000300: 6.057e1

GenotypeQuality
all individuals: 24
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 9.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1398
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

DP
type: SiteQuality
SIO_000300: 3.80966e5

BaseQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.290000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.434e-1

MQ
type: SiteQuality
SIO_000300: 5.728e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.15e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 126
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 1.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 19
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GenotypeQuality
all individuals: 186
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 360
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7662
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5064
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 156
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.74015e5

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

QD
type: SiteQuality
SIO_000300: 1.683e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.400000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 14
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 5.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 88
bin: 5.25e1
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GenotypeQuality
all individuals: 175
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 256
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6940
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 6.329113924050633e-3
allele num: 316
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.309999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.18287e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

QD
type: SiteQuality
SIO_000300: 1.403e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.31e0

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: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 6

GenotypeQuality
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bin: 5.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 3

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 9
bin: 9.25e1
variant carriers: 1

Other
type: Population
allele count: 1
allele frequency: 7.8125e-3
allele num: 128
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 4.347826086956522e-3
allele num: 230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 40
allele frequency: 9.818360333824251e-3
allele num: 4074
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.118178983473651e-4
allele num: 6414
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

QD
type: SiteQuality
SIO_000300: 1.539e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.06e-2

FS
type: SiteQuality
SIO_000300: 6.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e-1

DP
type: SiteQuality
SIO_000300: 1.91043e5

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 7.5e0
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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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bin: 2.25e1
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 129
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1112
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
all individuals: 306
bin: 3.75e1
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GenotypeQuality
all individuals: 364
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 294
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 110
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 1.287711552612215e-3
allele num: 5436
num of homozygotes: 1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.361e0

MQRankSum
type: SiteQuality
SIO_000300: 5.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.98e-2

QD
type: SiteQuality
SIO_000300: 1.625e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.19e-1

DP
type: SiteQuality
SIO_000300: 1.48558e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.92e-1

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 16
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 104
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5140
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3498
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 4.761904761904762e-3
allele num: 210
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-1

MQ
type: SiteQuality
SIO_000300: 5.845e1

DP
type: SiteQuality
SIO_000300: 1.39202e5

QD
type: SiteQuality
SIO_000300: 1.218e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.870000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.56e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.685e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.72e-1

GenotypeQuality
all individuals: 782
bin: 2.75e1
variant carriers: 3

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4154
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.052631578947368e-2
allele num: 190
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 84
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.270111183780249e-4
allele num: 3058
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

FS
type: SiteQuality
SIO_000300: 2.0438e1

VQSLOD
type: SiteQuality
SIO_000300: 4.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.91e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.286e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.002e0

DP
type: SiteQuality
SIO_000300: 1.24805e5

GenotypeQuality
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bin: 3.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.5e0
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 636
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3030
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 82
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.097e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.110000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 1.2478e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2940
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 70
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.28292e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.43e-2

QD
type: SiteQuality
SIO_000300: 1.035e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8920
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.729026766291497e-5
allele num: 21146
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2698
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2396
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.57e-1

FS
type: SiteQuality
SIO_000300: 1.853e0

MQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

DP
type: SiteQuality
SIO_000300: 7.64698e5

ClippingRankSum
type: SiteQuality
SIO_000300: 8.7e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.91e-2

QD
type: SiteQuality
SIO_000300: 1.31e1

GenotypeQuality
all individuals: 23529
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21700
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 3.61794500723589e-4
allele num: 2764
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2286
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4200
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8972
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 364
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

DP
type: SiteQuality
SIO_000300: 7.98967e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.68e-2

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.8e-2

QD
type: SiteQuality
SIO_000300: 1.212e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22242
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4278
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2364
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 7.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 8.13166e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.075e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1290
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 8.896797153024912e-5
allele num: 22480
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2838
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9080
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2412
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2644
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.23244e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

VQSLOD
type: SiteQuality
SIO_000300: 2.17e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.34e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 4.37e0

GenotypeQuality
all individuals: 1699
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2076
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1300
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1763
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2666
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 410
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27118
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5491
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4330
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2836
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2672
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2416
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9092
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.422821760283061e-5
allele num: 22610
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.991e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.33e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

DP
type: SiteQuality
SIO_000300: 8.28512e5

QD
type: SiteQuality
SIO_000300: 1.468e1

MQRankSum
type: SiteQuality
SIO_000300: -1.092e0

MQ
type: SiteQuality
SIO_000300: 5.855e1

VQSLOD
type: SiteQuality
SIO_000300: -1.828e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 1177
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3710
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1354
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3831
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4882
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1355
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28955
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.087192868014786e-4
allele num: 9198
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23782
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2966
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.55563e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.08e-2

MQ
type: SiteQuality
SIO_000300: 5.947e1

VQSLOD
type: SiteQuality
SIO_000300: -3.697e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.39e-1

QD
type: SiteQuality
SIO_000300: 1.709e1

GenotypeQuality
all individuals: 29033
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2805
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 408
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13316
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2670
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1070
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5462
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3740
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 2.017349203147065e-4
allele num: 29742
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

FS
type: SiteQuality
SIO_000300: 1.147e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.39e-1

QD
type: SiteQuality
SIO_000300: 1.209e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.46e0

DP
type: SiteQuality
SIO_000300: 9.71921e5

GenotypeQuality
all individuals: 1053
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2758
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 292
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1687
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2536
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2666
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 265
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28862
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1588
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14069
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3836
num of homozygotes: 0