12-53837339-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837339
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837339
    reference: chr 12
allele count: 7
allele frequency: 3.056234718826406e-4
allele num: 22904
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.184C>T
  hgvsp: ENSP00000448761.1:p.Pro62Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-124C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.226C>T
  hgvsp: ENSP00000446818.1:p.Pro76Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.256C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.184C>T
  hgvsp: ENSP00000447777.1:p.Pro62Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.34C>T
  hgvsp: ENSP00000448153.1:p.Pro12Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.88C>T
  hgvsp: ENSP00000448481.1:p.Pro30Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.20-12C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.184C>T
  hgvsp: ENSP00000447940.1:p.Pro62Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.34C>T
  hgvsp: ENSP00000369112.4:p.Pro12Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-294C>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.184C>T
  hgvsp: ENSP00000412064.2:p.Pro62Ser
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5371
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 37392
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10478
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro62Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

12-53837342-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837342
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837342
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 24600
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.37G>T
  hgvsp: ENSP00000369112.4:p.Val13Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-291G>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.20-9G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.187G>T
  hgvsp: ENSP00000448761.1:p.Val63Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.229G>T
  hgvsp: ENSP00000446818.1:p.Val77Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.187G>T
  hgvsp: ENSP00000447777.1:p.Val63Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.37G>T
  hgvsp: ENSP00000448153.1:p.Val13Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.187G>T
  hgvsp: ENSP00000412064.2:p.Val63Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.259G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.91G>T
  hgvsp: ENSP00000448481.1:p.Val31Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-121G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.187G>T
  hgvsp: ENSP00000447940.1:p.Val63Leu
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37333
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9798
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5672
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val63Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-53837348-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837348
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837348
    reference: chr 12
allele count: 1
allele frequency: 3.52013517319065e-5
allele num: 28408
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.193C>T
  hgvsp: ENSP00000412064.2:p.Gln65Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.265C>T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.193C>T
  hgvsp: ENSP00000447940.1:p.Gln65Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.193C>T
  hgvsp: ENSP00000447777.1:p.Gln65Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-285C>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.235C>T
  hgvsp: ENSP00000446818.1:p.Gln79Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.20-3C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.43C>T
  hgvsp: ENSP00000448153.1:p.Gln15Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.97C>T
  hgvsp: ENSP00000448481.1:p.Gln33Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.193C>T
  hgvsp: ENSP00000448761.1:p.Gln65Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-115C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.43C>T
  hgvsp: ENSP00000369112.4:p.Gln15Ter
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36768
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8600
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6527
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln65Ter
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

12-53837351-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837351
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837351
    reference: chr 12
allele count: 3
allele frequency: 1.005564121472146e-4
allele num: 29834
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.100C>T
  hgvsp: ENSP00000448481.1:p.Pro34Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.46C>T
  hgvsp: ENSP00000448153.1:p.Pro16Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.196C>T
  hgvsp: ENSP00000412064.2:p.Pro66Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.196C>T
  hgvsp: ENSP00000447940.1:p.Pro66Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.196C>T
  hgvsp: ENSP00000447777.1:p.Pro66Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.20C>T
  hgvsp: ENSP00000449513.1:p.Ala7Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.196C>T
  hgvsp: ENSP00000448761.1:p.Pro66Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-112C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.238C>T
  hgvsp: ENSP00000446818.1:p.Pro80Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.268C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.46C>T
  hgvsp: ENSP00000369112.4:p.Pro16Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-282C>T
  variant of: http://identifiers.org/hgnc/8648
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6800
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36512
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8040
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro66Ser
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

12-53837361-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837361
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837361
    reference: chr 12
allele count: 1
allele frequency: 2.589868434683518e-5
allele num: 38612
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.206C>T
  hgvsp: ENSP00000412064.2:p.Pro69Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.110C>T
  hgvsp: ENSP00000448481.1:p.Pro37Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.206C>T
  hgvsp: ENSP00000448761.1:p.Pro69Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-102C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.206C>T
  hgvsp: ENSP00000447940.1:p.Pro69Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.206C>T
  hgvsp: ENSP00000447777.1:p.Pro69Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-272C>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.30C>T
  hgvsp: ENST00000549068.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.56C>T
  hgvsp: ENSP00000448153.1:p.Pro19Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.248C>T
  hgvsp: ENSP00000446818.1:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.56C>T
  hgvsp: ENSP00000369112.4:p.Pro19Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.278C>T
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8195
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5890
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro69Leu
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-53837373-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837373
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837373
    reference: chr 12
allele count: 2
allele frequency: 3.943995267205679e-5
allele num: 50710
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.218C>T
  hgvsp: ENSP00000412064.2:p.Pro73Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.68C>T
  hgvsp: ENSP00000448153.1:p.Pro23Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.68C>T
  hgvsp: ENSP00000369112.4:p.Pro23Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.122C>T
  hgvsp: ENSP00000448481.1:p.Pro41Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.218C>T
  hgvsp: ENSP00000447940.1:p.Pro73Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.260C>T
  hgvsp: ENSP00000446818.1:p.Pro87Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.218C>T
  hgvsp: ENSP00000448761.1:p.Pro73Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-260C>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.42C>T
  hgvsp: ENST00000549068.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.218C>T
  hgvsp: ENSP00000447777.1:p.Pro73Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.290C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-90C>T
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11282
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31027
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8488
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro73Leu
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

12-53837374-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837374
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837374
    reference: chr 12
allele count: 29
allele frequency: 5.473557057113737e-4
allele num: 52982
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.219G>A
  hgvsp: ENST00000549740.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.43G>A
  hgvsp: ENSP00000449513.1:p.Val15Ile
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.291G>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.219G>A
  hgvsp: ENST00000429243.2:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.219G>A
  hgvsp: ENST00000549924.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.69G>A
  hgvsp: ENST00000379786.4:c.69G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.261G>A
  hgvsp: ENST00000547368.1:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.219G>A
  hgvsp: ENST00000549135.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-259G>A
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-89G>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.123G>A
  hgvsp: ENST00000551003.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.69G>A
  hgvsp: ENST00000549581.1:c.69G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8343
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12523
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 30174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Val15Ile
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/12-53837385-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837385
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837385
    reference: chr 12
allele count: 1
allele frequency: 1.525041176111755e-5
allele num: 65572
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-78A>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.230A>C
  hgvsp: ENSP00000448761.1:p.Tyr77Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.80A>C
  hgvsp: ENSP00000369112.4:p.Tyr27Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.230A>C
  hgvsp: ENSP00000412064.2:p.Tyr77Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.54A>C
  hgvsp: ENST00000549068.1:c.54A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.80A>C
  hgvsp: ENSP00000448153.1:p.Tyr27Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.230A>C
  hgvsp: ENSP00000447777.1:p.Tyr77Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-248A>C
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.272A>C
  hgvsp: ENSP00000446818.1:p.Tyr91Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.134A>C
  hgvsp: ENSP00000448481.1:p.Tyr45Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.230A>C
  hgvsp: ENSP00000447940.1:p.Tyr77Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.302A>C
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7681
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr77Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

12-53837391-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837391
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837391
    reference: chr 12
allele count: 1
allele frequency: 1.376462491397109e-5
allele num: 72650
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.278C>T
  hgvsp: ENSP00000446818.1:p.Pro93Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.236C>T
  hgvsp: ENSP00000412064.2:p.Pro79Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-242C>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.236C>T
  hgvsp: ENSP00000448761.1:p.Pro79Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.140C>T
  hgvsp: ENSP00000448481.1:p.Pro47Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.308C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.236C>T
  hgvsp: ENSP00000447777.1:p.Pro79Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-72C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.236C>T
  hgvsp: ENSP00000447940.1:p.Pro79Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.60C>T
  hgvsp: ENST00000549068.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.86C>T
  hgvsp: ENSP00000448153.1:p.Pro29Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.86C>T
  hgvsp: ENSP00000369112.4:p.Pro29Leu
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 7129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4257
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro79Leu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

12-53837398-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837398
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837398
    reference: chr 12
allele count: 1
allele frequency: 1.152206475400392e-5
allele num: 86790
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-65C>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.243C>G
  hgvsp: ENSP00000447940.1:p.Tyr81Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-235C>G
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.285C>G
  hgvsp: ENSP00000446818.1:p.Tyr95Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.243C>G
  hgvsp: ENSP00000412064.2:p.Tyr81Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.243C>G
  hgvsp: ENSP00000447777.1:p.Tyr81Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.315C>G
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.243C>G
  hgvsp: ENSP00000448761.1:p.Tyr81Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.93C>G
  hgvsp: ENSP00000448153.1:p.Tyr31Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.147C>G
  hgvsp: ENSP00000448481.1:p.Tyr49Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.93C>G
  hgvsp: ENSP00000369112.4:p.Tyr31Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.67C>G
  hgvsp: ENSP00000449513.1:p.Pro23Ala
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 5841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16032
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29397
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr81Ter
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

12-53837403-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837403
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837403
    reference: chr 12
allele count: 1
allele frequency: 1.005489975264947e-5
allele num: 99454
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.152C>T
  hgvsp: ENSP00000448481.1:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.290C>T
  hgvsp: ENSP00000446818.1:p.Pro97Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-60C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-230C>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.248C>T
  hgvsp: ENSP00000412064.2:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.248C>T
  hgvsp: ENSP00000447940.1:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.72C>T
  hgvsp: ENST00000549068.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.248C>T
  hgvsp: ENSP00000447777.1:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.98C>T
  hgvsp: ENSP00000448153.1:p.Pro33Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.98C>T
  hgvsp: ENSP00000369112.4:p.Pro33Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.248C>T
  hgvsp: ENSP00000448761.1:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.320C>T
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10038
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro83Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

12-53837405-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837405
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837405
    reference: chr 12
allele count: 2
allele frequency: 1.91255785487511e-5
allele num: 104572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.250C>T
  hgvsp: ENSP00000448761.1:p.Pro84Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.100C>T
  hgvsp: ENSP00000369112.4:p.Pro34Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.292C>T
  hgvsp: ENSP00000446818.1:p.Pro98Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.250C>T
  hgvsp: ENSP00000412064.2:p.Pro84Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.154C>T
  hgvsp: ENSP00000448481.1:p.Pro52Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.250C>T
  hgvsp: ENSP00000447777.1:p.Pro84Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.74C>T
  hgvsp: ENSP00000449513.1:p.Ala25Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-228C>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.100C>T
  hgvsp: ENSP00000448153.1:p.Pro34Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.250C>T
  hgvsp: ENSP00000447940.1:p.Pro84Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-58C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.322C>T
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7680
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro84Ser
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

12-53837409-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837409
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837409
    reference: chr 12
allele count: 1
allele frequency: 9.084797499863727e-6
allele num: 110074
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.158C>T
  hgvsp: ENSP00000448481.1:p.Ala53Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.104C>T
  hgvsp: ENSP00000369112.4:p.Ala35Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.254C>T
  hgvsp: ENSP00000412064.2:p.Ala85Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.254C>T
  hgvsp: ENSP00000447777.1:p.Ala85Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.296C>T
  hgvsp: ENSP00000446818.1:p.Ala99Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-54C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.104C>T
  hgvsp: ENSP00000448153.1:p.Ala35Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.254C>T
  hgvsp: ENSP00000447940.1:p.Ala85Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.78C>T
  hgvsp: ENST00000549068.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-224C>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.326C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.254C>T
  hgvsp: ENSP00000448761.1:p.Ala85Val
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5045
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42342
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9025
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala85Val
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

12-53837424-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837424
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837424
    reference: chr 12
allele count: 1
allele frequency: 8.561497234636393e-6
allele num: 116802
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.341C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.119C>T
  hgvsp: ENSP00000448153.1:p.Pro40Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.269C>T
  hgvsp: ENSP00000448761.1:p.Pro90Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.173C>T
  hgvsp: ENSP00000448481.1:p.Pro58Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.269C>T
  hgvsp: ENSP00000447777.1:p.Pro90Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.311C>T
  hgvsp: ENSP00000446818.1:p.Pro104Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.269C>T
  hgvsp: ENSP00000447940.1:p.Pro90Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.93C>T
  hgvsp: ENST00000549068.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.119C>T
  hgvsp: ENSP00000369112.4:p.Pro40Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-39C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.269C>T
  hgvsp: ENSP00000412064.2:p.Pro90Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-209C>T
  variant of: http://identifiers.org/hgnc/8648
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro90Leu
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

12-53837427-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837427
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837427
    reference: chr 12
allele count: 1
allele frequency: 8.525876033762469e-6
allele num: 117290
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.344T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.96T>C
  hgvsp: ENST00000549068.1:c.96T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.272T>C
  hgvsp: ENSP00000412064.2:p.Val91Ala
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-36T>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.272T>C
  hgvsp: ENSP00000447940.1:p.Val91Ala
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.122T>C
  hgvsp: ENSP00000369112.4:p.Val41Ala
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.122T>C
  hgvsp: ENSP00000448153.1:p.Val41Ala
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.272T>C
  hgvsp: ENSP00000448761.1:p.Val91Ala
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.176T>C
  hgvsp: ENSP00000448481.1:p.Val59Ala
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.272T>C
  hgvsp: ENSP00000447777.1:p.Val91Ala
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.314T>C
  hgvsp: ENSP00000446818.1:p.Val105Ala
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-206T>C
  variant of: http://identifiers.org/hgnc/8648
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val91Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

12-53837432-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837432
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837432
    reference: chr 12
allele count: 6
allele frequency: 5.087677644744429e-5
allele num: 117932
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.127C>T
  hgvsp: ENSP00000448153.1:p.Pro43Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.349C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.181C>T
  hgvsp: ENSP00000448481.1:p.Pro61Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.277C>T
  hgvsp: ENSP00000412064.2:p.Pro93Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.127C>T
  hgvsp: ENSP00000369112.4:p.Pro43Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.101C>T
  hgvsp: ENSP00000449513.1:p.Ser34Phe
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.319C>T
  hgvsp: ENSP00000446818.1:p.Pro107Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-31C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-201C>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.277C>T
  hgvsp: ENSP00000447940.1:p.Pro93Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.277C>T
  hgvsp: ENSP00000447777.1:p.Pro93Ser
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.277C>T
  hgvsp: ENSP00000448761.1:p.Pro93Ser
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro93Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-53837440-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837440
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837440
    reference: chr 12
allele count: 1
allele frequency: 8.433836552247617e-6
allele num: 118570
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.135T>C
  hgvsp: ENST00000379786.4:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.135T>C
  hgvsp: ENST00000549581.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.285T>C
  hgvsp: ENST00000549924.1:c.285T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-23T>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.189T>C
  hgvsp: ENST00000551003.1:c.189T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.109T>C
  hgvsp: ENSP00000449513.1:p.Ser37Pro
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.327T>C
  hgvsp: ENST00000547368.1:c.327T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.285T>C
  hgvsp: ENST00000429243.2:c.285T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.285T>C
  hgvsp: ENST00000549740.1:c.285T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.285T>C
  hgvsp: ENST00000549135.1:c.285T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-193T>C
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.357T>C
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser37Pro
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

12-53837442-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837442
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837442
    reference: chr 12
allele count: 1
allele frequency: 8.427865895797866e-6
allele num: 118654
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.287C>T
  hgvsp: ENSP00000447940.1:p.Pro96Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.287C>T
  hgvsp: ENSP00000447777.1:p.Pro96Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.137C>T
  hgvsp: ENSP00000448153.1:p.Pro46Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.137C>T
  hgvsp: ENSP00000369112.4:p.Pro46Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-191C>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.191C>T
  hgvsp: ENSP00000448481.1:p.Pro64Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.287C>T
  hgvsp: ENSP00000448761.1:p.Pro96Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.287C>T
  hgvsp: ENSP00000412064.2:p.Pro96Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.329C>T
  hgvsp: ENSP00000446818.1:p.Pro110Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.111C>T
  hgvsp: ENST00000549068.1:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-21C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.359C>T
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro96Leu
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

12-53837454-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837454
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837454
    reference: chr 12
allele count: 1
allele frequency: 8.366100560528738e-6
allele num: 119530
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.149G>T
  hgvsp: ENSP00000448153.1:p.Gly50Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-179G>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.299G>T
  hgvsp: ENSP00000447777.1:p.Gly100Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.299G>T
  hgvsp: ENSP00000448761.1:p.Gly100Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.299G>T
  hgvsp: ENSP00000447940.1:p.Gly100Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.341G>T
  hgvsp: ENSP00000446818.1:p.Gly114Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.299G>T
  hgvsp: ENSP00000412064.2:p.Gly100Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.371G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-9G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.203G>T
  hgvsp: ENSP00000448481.1:p.Gly68Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.149G>T
  hgvsp: ENSP00000369112.4:p.Gly50Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.123G>T
  hgvsp: ENSP00000449513.1:p.Trp41Cys
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11242
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly100Val
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/12-53837456-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837456
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837456
    reference: chr 12
allele count: 1
allele frequency: 8.358268835358821e-6
allele num: 119642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.301C>A
  hgvsp: ENSP00000447940.1:p.Pro101Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.343C>A
  hgvsp: ENSP00000446818.1:p.Pro115Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.151C>A
  hgvsp: ENSP00000448153.1:p.Pro51Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.373C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.301C>A
  hgvsp: ENSP00000448761.1:p.Pro101Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.301C>A
  hgvsp: ENSP00000447777.1:p.Pro101Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-7C>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-177C>A
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.205C>A
  hgvsp: ENSP00000448481.1:p.Pro69Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.151C>A
  hgvsp: ENSP00000369112.4:p.Pro51Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.301C>A
  hgvsp: ENSP00000412064.2:p.Pro101Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.125C>A
  hgvsp: ENSP00000449513.1:p.Thr42Asn
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11280
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro101Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/12-53837458-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837458
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837458
    reference: chr 12
allele count: 143
allele frequency: 1.194034835757586e-3
allele num: 119762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-175A>C
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.303A>C
  hgvsp: ENST00000549924.1:c.303A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.303A>C
  hgvsp: ENST00000429243.2:c.303A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.127A>C
  hgvsp: ENSP00000449513.1:p.Ser43Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.303A>C
  hgvsp: ENST00000549740.1:c.303A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.345A>C
  hgvsp: ENST00000547368.1:c.345A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.153A>C
  hgvsp: ENST00000549581.1:c.153A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.207A>C
  hgvsp: ENST00000551003.1:c.207A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.375A>C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-5A>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.303A>C
  hgvsp: ENST00000549135.1:c.303A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.153A>C
  hgvsp: ENST00000379786.4:c.153A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11305
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45831
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 3.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
hgvs: p.Ser43Arg
num of homozygotes: 3
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

12-53837458-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837458
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837458
    reference: chr 12
allele count: 2
allele frequency: 1.669978791269351e-5
allele num: 119762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.127A>G
  hgvsp: ENSP00000449513.1:p.Ser43Gly
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.303A>G
  hgvsp: ENST00000549135.1:c.303A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-5A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.153A>G
  hgvsp: ENST00000379786.4:c.153A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-175A>G
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.153A>G
  hgvsp: ENST00000549581.1:c.153A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.303A>G
  hgvsp: ENST00000549924.1:c.303A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.345A>G
  hgvsp: ENST00000547368.1:c.345A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.303A>G
  hgvsp: ENST00000549740.1:c.303A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.207A>G
  hgvsp: ENST00000551003.1:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.303A>G
  hgvsp: ENST00000429243.2:c.303A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.375A>G
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser43Gly
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

12-53837462-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837462
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837462
    reference: chr 12
allele count: 9
allele frequency: 7.503251408943875e-5
allele num: 119948
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.157G>C
  hgvsp: ENSP00000448153.1:p.Val53Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.307G>C
  hgvsp: ENSP00000447777.1:p.Val103Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.157G>C
  hgvsp: ENSP00000369112.4:p.Val53Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.211G>C
  hgvsp: ENSP00000448481.1:p.Val71Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-171G>C
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.307G>C
  hgvsp: ENSP00000447940.1:p.Val103Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.349G>C
  hgvsp: ENSP00000446818.1:p.Val117Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.307G>C
  hgvsp: ENSP00000448761.1:p.Val103Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.20-1G>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.379G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.131G>C
  hgvsp: ENSP00000449513.1:p.Ser44Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.307G>C
  hgvsp: ENSP00000412064.2:p.Val103Leu
  variant of: http://identifiers.org/hgnc/24528
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45871
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.20-1G>C
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS

12-53837465-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837465
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837465
    reference: chr 12
allele count: 1
allele frequency: 8.334722453742291e-6
allele num: 119980
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.310A>G
  hgvsp: ENSP00000447777.1:p.Ile104Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.310A>G
  hgvsp: ENSP00000447940.1:p.Ile104Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-168A>G
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.310A>G
  hgvsp: ENSP00000448761.1:p.Ile104Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.160A>G
  hgvsp: ENSP00000448153.1:p.Ile54Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.352A>G
  hgvsp: ENSP00000446818.1:p.Ile118Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.134A>G
  hgvsp: ENSP00000449513.1:p.Asp45Gly
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.214A>G
  hgvsp: ENSP00000448481.1:p.Ile72Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.382A>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.310A>G
  hgvsp: ENSP00000412064.2:p.Ile104Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.22A>G
  hgvsp: ENSP00000450334.1:p.Ile8Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.160A>G
  hgvsp: ENSP00000369112.4:p.Ile54Val
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile104Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

12-53837469-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837469
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837469
    reference: chr 12
allele count: 1
allele frequency: 8.333888925928395e-6
allele num: 119992
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.164T>C
  hgvsp: ENSP00000448153.1:p.Val55Ala
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.138T>C
  hgvsp: ENST00000549068.1:c.138T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.314T>C
  hgvsp: ENSP00000448761.1:p.Val105Ala
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.314T>C
  hgvsp: ENSP00000412064.2:p.Val105Ala
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-164T>C
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.218T>C
  hgvsp: ENSP00000448481.1:p.Val73Ala
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.314T>C
  hgvsp: ENSP00000447777.1:p.Val105Ala
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.164T>C
  hgvsp: ENSP00000369112.4:p.Val55Ala
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.26T>C
  hgvsp: ENSP00000450334.1:p.Val9Ala
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.314T>C
  hgvsp: ENSP00000447940.1:p.Val105Ala
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.356T>C
  hgvsp: ENSP00000446818.1:p.Val119Ala
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.386T>C
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val105Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS

12-53837479-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837479
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837479
    reference: chr 12
allele count: 1
allele frequency: 8.400961069946402e-6
allele num: 119034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.324G>T
  hgvsp: ENSP00000447940.1:p.Lys108Asn
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.228G>T
  hgvsp: ENSP00000448481.1:p.Lys76Asn
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.148G>T
  hgvsp: ENSP00000449513.1:p.Asp50Tyr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.324G>T
  hgvsp: ENSP00000447777.1:p.Lys108Asn
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.324G>T
  hgvsp: ENSP00000412064.2:p.Lys108Asn
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.174G>T
  hgvsp: ENSP00000448153.1:p.Lys58Asn
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.324G>T
  hgvsp: ENSP00000448761.1:p.Lys108Asn
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.366G>T
  hgvsp: ENSP00000446818.1:p.Lys122Asn
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.174G>T
  hgvsp: ENSP00000369112.4:p.Lys58Asn
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.36G>T
  hgvsp: ENSP00000450334.1:p.Lys12Asn
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.396G>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-154G>T
  variant of: http://identifiers.org/hgnc/8648
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys108Asn
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

12-53837483-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837483
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837483
    reference: chr 12
allele count: 1
allele frequency: 8.429144610404936e-6
allele num: 118636
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.328C>T
  hgvsp: ENSP00000412064.2:p.Gln110Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.370C>T
  hgvsp: ENSP00000446818.1:p.Gln124Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.152C>T
  hgvsp: ENSP00000449513.1:p.Ala51Val
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.178C>T
  hgvsp: ENSP00000369112.4:p.Gln60Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.328C>T
  hgvsp: ENSP00000447777.1:p.Gln110Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.178C>T
  hgvsp: ENSP00000448153.1:p.Gln60Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.40C>T
  hgvsp: ENSP00000450334.1:p.Gln14Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.328C>T
  hgvsp: ENSP00000448761.1:p.Gln110Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.232C>T
  hgvsp: ENSP00000448481.1:p.Gln78Ter
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.400C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-150C>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.328C>T
  hgvsp: ENSP00000447940.1:p.Gln110Ter
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43872
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln110Ter
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP

12-53837493-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837493
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837493
    reference: chr 12
allele count: 1
allele frequency: 8.655610566769381e-6
allele num: 115532
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.338T>A
  hgvsp: ENSP00000412064.2:p.Met113Lys
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.162T>A
  hgvsp: ENSP00000449513.1:p.Asn54Lys
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.380T>A
  hgvsp: ENSP00000446818.1:p.Met127Lys
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.338T>A
  hgvsp: ENSP00000447940.1:p.Met113Lys
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.188T>A
  hgvsp: ENSP00000448153.1:p.Met63Lys
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.188T>A
  hgvsp: ENSP00000369112.4:p.Met63Lys
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.338T>A
  hgvsp: ENSP00000447777.1:p.Met113Lys
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.50T>A
  hgvsp: ENSP00000450334.1:p.Met17Lys
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.338T>A
  hgvsp: ENSP00000448761.1:p.Met113Lys
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.410T>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.242T>A
  hgvsp: ENSP00000448481.1:p.Met81Lys
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-140T>A
  variant of: http://identifiers.org/hgnc/8648
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11251
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met113Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD

12-53837504-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837504
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837504
    reference: chr 12
allele count: 1
allele frequency: 9.12275580207269e-6
allele num: 109616
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.421C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.349C>T
  hgvsp: ENSP00000448761.1:p.His117Tyr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-129C>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.199C>T
  hgvsp: ENSP00000448153.1:p.His67Tyr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.61C>T
  hgvsp: ENSP00000450334.1:p.His21Tyr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.349C>T
  hgvsp: ENSP00000447940.1:p.His117Tyr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.391C>T
  hgvsp: ENSP00000446818.1:p.His131Tyr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.349C>T
  hgvsp: ENSP00000412064.2:p.His117Tyr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.349C>T
  hgvsp: ENSP00000447777.1:p.His117Tyr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.199C>T
  hgvsp: ENSP00000369112.4:p.His67Tyr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.253C>T
  hgvsp: ENSP00000448481.1:p.His85Tyr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.173C>T
  hgvsp: ENSP00000449513.1:p.Ser58Leu
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His117Tyr
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

12-53837505-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837505
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837505
    reference: chr 12
allele count: 1
allele frequency: 9.200647725599883e-6
allele num: 108688
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.350A>T
  hgvsp: ENSP00000412064.2:p.His117Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-128A>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.62A>T
  hgvsp: ENSP00000450334.1:p.His21Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.392A>T
  hgvsp: ENSP00000446818.1:p.His131Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.200A>T
  hgvsp: ENSP00000448153.1:p.His67Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.350A>T
  hgvsp: ENSP00000447940.1:p.His117Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.350A>T
  hgvsp: ENSP00000447777.1:p.His117Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.200A>T
  hgvsp: ENSP00000369112.4:p.His67Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.174A>T
  hgvsp: ENST00000549068.1:c.174A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.422A>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.350A>T
  hgvsp: ENSP00000448761.1:p.His117Leu
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.254A>T
  hgvsp: ENSP00000448481.1:p.His85Leu
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 34403
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10309
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His117Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-53837515-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837515
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837515
    reference: chr 12
allele count: 1
allele frequency: 1.018807180553009e-5
allele num: 98154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*7G>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.72G>A
  hgvsp: ENSP00000450334.1:p.Met24Ile
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-118G>A
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.360G>A
  hgvsp: ENSP00000448761.1:p.Met120Ile
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.360G>A
  hgvsp: ENSP00000447940.1:p.Met120Ile
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.210G>A
  hgvsp: ENSP00000369112.4:p.Met70Ile
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.360G>A
  hgvsp: ENSP00000447777.1:p.Met120Ile
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.210G>A
  hgvsp: ENSP00000448153.1:p.Met70Ile
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.264G>A
  hgvsp: ENSP00000448481.1:p.Met88Ile
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.360G>A
  hgvsp: ENSP00000412064.2:p.Met120Ile
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.402G>A
  hgvsp: ENSP00000446818.1:p.Met134Ile
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.432G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11073
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10462
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8561
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met120Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

12-53837518-CAAGCACCAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837518
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837509
    reference: chr 12
allele count: 9
allele frequency: 9.456562854621106e-5
allele num: 95172
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.372_380delAAAGCACCA
  hgvsp: ENSP00000448761.1:p.Gln124_His126del
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.372_380delAAAGCACCA
  hgvsp: ENSP00000447777.1:p.Gln124_His126del
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.276_284delAAAGCACCA
  hgvsp: ENSP00000448481.1:p.Gln92_His94del
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.84_92delAAAGCACCA
  hgvsp: ENSP00000450334.1:p.Gln28_His30del
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.444_452delAAAGCACCA
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.372_380delAAAGCACCA
  hgvsp: ENSP00000447940.1:p.Gln124_His126del
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.414_422delAAAGCACCA
  hgvsp: ENSP00000446818.1:p.Gln138_His140del
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.222_230delAAAGCACCA
  hgvsp: ENSP00000448153.1:p.Gln74_His76del
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.222_230delAAAGCACCA
  hgvsp: ENSP00000369112.4:p.Gln74_His76del
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.372_380delAAAGCACCA
  hgvsp: ENSP00000412064.2:p.Gln124_His126del
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*19_*27delAAAGCACCA
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 12397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 23726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11629
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln124_His126del
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: CAAGCACCAA
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-53837523-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837523
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837523
    reference: chr 12
allele count: 1
allele frequency: 1.138018936635106e-5
allele num: 87872
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.410A>G
  hgvsp: ENSP00000446818.1:p.His137Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.272A>G
  hgvsp: ENSP00000448481.1:p.His91Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.218A>G
  hgvsp: ENSP00000448153.1:p.His73Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.368A>G
  hgvsp: ENSP00000412064.2:p.His123Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.368A>G
  hgvsp: ENSP00000447777.1:p.His123Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.218A>G
  hgvsp: ENSP00000369112.4:p.His73Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.80A>G
  hgvsp: ENSP00000450334.1:p.His27Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.368A>G
  hgvsp: ENSP00000447940.1:p.His123Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.440A>G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-110A>G
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.368A>G
  hgvsp: ENSP00000448761.1:p.His123Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*15A>G
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13945
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His123Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

12-53837532-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837532
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837532
    reference: chr 12
allele count: 1
allele frequency: 1.28083612982555e-5
allele num: 78074
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.449A>G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-101A>G
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.377A>G
  hgvsp: ENSP00000447940.1:p.His126Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.227A>G
  hgvsp: ENSP00000448153.1:p.His76Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.419A>G
  hgvsp: ENSP00000446818.1:p.His140Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.377A>G
  hgvsp: ENSP00000412064.2:p.His126Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*24A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.227A>G
  hgvsp: ENSP00000369112.4:p.His76Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.377A>G
  hgvsp: ENSP00000447777.1:p.His126Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.89A>G
  hgvsp: ENSP00000450334.1:p.His30Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.377A>G
  hgvsp: ENSP00000448761.1:p.His126Arg
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.281A>G
  hgvsp: ENSP00000448481.1:p.His94Arg
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His126Arg
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/12-53837535-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837535
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837535
    reference: chr 12
allele count: 1
allele frequency: 1.288593371475697e-5
allele num: 77604
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*27A>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.380A>C
  hgvsp: ENSP00000412064.2:p.His127Pro
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.230A>C
  hgvsp: ENSP00000369112.4:p.His77Pro
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.284A>C
  hgvsp: ENSP00000448481.1:p.His95Pro
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.230A>C
  hgvsp: ENSP00000448153.1:p.His77Pro
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.422A>C
  hgvsp: ENSP00000446818.1:p.His141Pro
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.92A>C
  hgvsp: ENSP00000450334.1:p.His31Pro
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.380A>C
  hgvsp: ENSP00000448761.1:p.His127Pro
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-98A>C
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.380A>C
  hgvsp: ENSP00000447940.1:p.His127Pro
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.380A>C
  hgvsp: ENSP00000447777.1:p.His127Pro
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.452A>C
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 15168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15170
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His127Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/12-53837547-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837547
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837547
    reference: chr 12
allele count: 6
allele frequency: 8.352125615969264e-5
allele num: 71838
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.392A>C
  hgvsp: ENSP00000447940.1:p.Lys131Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-86A>C
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.242A>C
  hgvsp: ENSP00000448153.1:p.Lys81Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.392A>C
  hgvsp: ENSP00000412064.2:p.Lys131Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.392A>C
  hgvsp: ENSP00000447777.1:p.Lys131Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.104A>C
  hgvsp: ENSP00000450334.1:p.Lys35Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.392A>C
  hgvsp: ENSP00000448761.1:p.Lys131Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.242A>C
  hgvsp: ENSP00000369112.4:p.Lys81Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*39A>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.434A>C
  hgvsp: ENSP00000446818.1:p.Lys145Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.296A>C
  hgvsp: ENSP00000448481.1:p.Lys99Thr
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.464A>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16079
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4316
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12466
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20718
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys131Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/12-53837549-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837549
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837549
    reference: chr 12
allele count: 6
allele frequency: 8.468356574267488e-5
allele num: 70852
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.394C>A
  hgvsp: ENSP00000448761.1:p.His132Asn
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*41C>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.394C>A
  hgvsp: ENSP00000447777.1:p.His132Asn
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.394C>A
  hgvsp: ENSP00000412064.2:p.His132Asn
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.436C>A
  hgvsp: ENSP00000446818.1:p.His146Asn
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.244C>A
  hgvsp: ENSP00000448153.1:p.His82Asn
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.298C>A
  hgvsp: ENSP00000448481.1:p.His100Asn
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-84C>A
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.106C>A
  hgvsp: ENSP00000450334.1:p.His36Asn
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.394C>A
  hgvsp: ENSP00000447940.1:p.His132Asn
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.466C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.244C>A
  hgvsp: ENSP00000369112.4:p.His82Asn
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4012
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16202
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12052
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20831
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His132Asn
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

12-53837560-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837560
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837560
    reference: chr 12
allele count: 1
allele frequency: 1.652291728627607e-5
allele num: 60522
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.402+3C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+3C>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.306+3C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+3C>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.252+3C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.405C>T
  hgvsp: ENST00000549740.1:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.402+3C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*49+3C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.444+3C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.114+3C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.252+3C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.402+3C>T
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16066
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.474+3C>T
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

12-53837600-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837600
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837598
    reference: chr 12
allele count: 1
allele frequency: 4.434983147064041e-5
allele num: 22548
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.402+46_402+47delAG
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.252+46_252+47delAG
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.306+46_306+47delAG
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.114+46_114+47delAG
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.402+46_402+47delAG
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*49+46_*49+47delAG
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.448_449delAG
  hgvsp: ENSP00000447940.1:p.Arg150GlyfsTer33
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.444+46_444+47delAG
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.402+46_402+47delAG
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+46_-76+47delAG
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+46_474+47delAG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.252+46_252+47delAG
  variant of: http://identifiers.org/hgnc/24528
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 29219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15522
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg150GlyfsTer33
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: CAG
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

12-53837614-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837614
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837614
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 16762
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+57A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.402+57A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.444+57A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.*3A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.402+57A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*49+57A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+57A>G
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.252+57A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.402+57A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.306+57A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.114+57A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.252+57A>G
  variant of: http://identifiers.org/hgnc/24528
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32865
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11383
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/12-53837617-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837617
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837617
    reference: chr 12
allele count: 3
allele frequency: 1.93473494131304e-4
allele num: 15506
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.*6C>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.252+60C>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+60C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.444+60C>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.252+60C>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+60C>A
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.306+60C>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*49+60C>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.114+60C>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.402+60C>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.402+60C>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.402+60C>A
  variant of: http://identifiers.org/hgnc/24528
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33251
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

12-53837640-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837640
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837640
    reference: chr 12
allele count: 1
allele frequency: 8.791981712678038e-5
allele num: 11374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+83A>G
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.252+83A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.*29A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*49+83A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.306+83A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.402+83A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.444+83A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+83A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.114+83A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.402+83A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.252+83A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.402+83A>G
  variant of: http://identifiers.org/hgnc/24528
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7069
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-53837653-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53837653
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53837653
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 10162
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.306+96G>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447940
  ensembl transcript: ENST00000549740
  gene symbol: PRR13
  hgvsc: ENST00000549740.1:c.*42G>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*49+96G>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.402+96G>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.402+96G>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+96G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+96G>C
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.114+96G>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.444+96G>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.252+96G>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.402+96G>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.252+96G>C
  variant of: http://identifiers.org/hgnc/24528
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 31992
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

12-53839748-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839748
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839748
    reference: chr 12
allele count: 1
allele frequency: 8.400961069946402e-6
allele num: 119034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.307-51T>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.253-51T>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.115-51T>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+2191T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+2191T>A
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.445-51T>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.253-51T>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*50-51T>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.403-51T>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.403-51T>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.403-51T>A
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8867
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-53839753-T-TGGATCTGATGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839753
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839764
    reference: chr 12
allele count: 1
allele frequency: 8.475150857685267e-6
allele num: 117992
alternate allele: TGGATCTGATGC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4582
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8886
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4019
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4714
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1300
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1883
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1966
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

12-53839755-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839755
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839755
    reference: chr 12
allele count: 7
allele frequency: 5.940459621847313e-5
allele num: 117836
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.403-44G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+2198G>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.253-44G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.403-44G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+2198G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*50-44G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.253-44G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.307-44G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.445-44G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.403-44G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.115-44G>T
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4702
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4582
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4885
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8904
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4038
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1384
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/12-53839756-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839756
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839756
    reference: chr 12
allele count: 11
allele frequency: 9.434771421219658e-5
allele num: 116590
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.403-43A>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.307-43A>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.445-43A>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.403-43A>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.253-43A>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+2199A>C
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.403-43A>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+2199A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.253-43A>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*50-43A>C
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.115-43A>C
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4905
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4034
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8939
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4679
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2617
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

12-53839766-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839766
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839766
    reference: chr 12
allele count: 134
allele frequency: 1.200308138805783e-3
allele num: 111638
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.403-33A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+2209A>G
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.307-33A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.403-33A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.115-33A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.403-33A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.253-33A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.253-33A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+2209A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.445-33A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*50-33A>G
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 9699
  bin: 9.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4158
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3345
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

12-53839766-ATCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839766
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839763
    reference: chr 12
allele count: 1
allele frequency: 8.957523423923754e-6
allele num: 111638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.253-28_253-26delCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.403-28_403-26delCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.445-28_445-26delCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.115-28_115-26delCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*50-28_*50-26delCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+2214_474+2216delCTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+2214_-76+2216delCTT
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.403-28_403-26delCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.403-28_403-26delCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.253-28_253-26delCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.307-28_307-26delCTT
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3345
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9699
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1527
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: ATCT
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

12-53839770-T-TCTTTCCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839770
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839777
    reference: chr 12
allele count: 22462
allele frequency: 1.880420587348893e-1
allele num: 119452
alternate allele: TCTTTCCC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.253-11_253-5dupTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.115-11_115-5dupTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.445-11_445-5dupTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.403-11_403-5dupTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.253-11_253-5dupTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.307-11_307-5dupTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.403-11_403-5dupTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.403-11_403-5dupTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*50-11_*50-5dupTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 3.75e1
  variant carriers: 943
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 1197
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 4.25e1
  variant carriers: 960
genotype depth: GenotypeDepth
  all individuals: 3720
  bin: 4.75e1
  variant carriers: 955
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 8.75e1
  variant carriers: 985
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 3.25e1
  variant carriers: 925
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 5.75e1
  variant carriers: 1178
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 2.75e1
  variant carriers: 839
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 166
genotype depth: GenotypeDepth
  all individuals: 4026
  bin: 5.25e1
  variant carriers: 1029
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 2.25e1
  variant carriers: 563
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 7.75e1
  variant carriers: 1290
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.75e1
  variant carriers: 345
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 6.25e1
  variant carriers: 1307
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 6.75e1
  variant carriers: 1363
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 9.25e1
  variant carriers: 774
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 7.25e1
  variant carriers: 1384
genotype depth: GenotypeDepth
  all individuals: 9707
  bin: 9.75e1
  variant carriers: 4128
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.25e1
  variant carriers: 93
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 7.25e1
  variant carriers: 119
num of homozygotes: 2359
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

12-53839770-TCTTTCCC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839770
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839763
    reference: chr 12
allele count: 403
allele frequency: 3.373740079697284e-3
allele num: 119452
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*50-11_*50-5delTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.307-11_307-5delTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.253-11_253-5delTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.445-11_445-5delTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.115-11_115-5delTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.253-11_253-5delTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.403-11_403-5delTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.403-11_403-5delTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.403-11_403-5delTCCCCTT
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 3.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 9707
  bin: 9.75e1
  variant carriers: 171
genotype depth: GenotypeDepth
  all individuals: 4026
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 3.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 7.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 6.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 6.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 7.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 3720
  bin: 4.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 9.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 8.75e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: TCTTTCCC
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

12-53839770-T-TCTTTCCCCTTTCCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839770
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839784
    reference: chr 12
allele count: 1
allele frequency: 8.371563473194253e-6
allele num: 119452
alternate allele: TCTTTCCCCTTTCCC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3720
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4026
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9707
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1144
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

12-53839773-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839773
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839773
    reference: chr 12
allele count: 19
allele frequency: 1.600808829724492e-4
allele num: 118690
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.115-26T>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*50-26T>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.403-26T>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.307-26T>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.403-26T>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.253-26T>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.403-26T>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+2216T>A
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.253-26T>A
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+2216T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.445-26T>A
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8083
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4762
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3797
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 3
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

12-53839775-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839775
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839775
    reference: chr 12
allele count: 27
allele frequency: 2.283491204330176e-4
allele num: 118240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.445-24C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.253-24C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+2218C>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.403-24C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.307-24C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+2218C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.403-24C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.253-24C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*50-24C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.403-24C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.115-24C>T
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8329
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4326
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4713
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 5
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

12-53839777-C-CCTTTCCG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839777
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839784
    reference: chr 12
allele count: 1
allele frequency: 8.479031355457952e-6
allele num: 117938
alternate allele: CCTTTCCG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.115-16_115-15insGCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.253-16_253-15insGCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*50-16_*50-15insGCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.403-16_403-15insGCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.253-16_253-15insGCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.403-16_403-15insGCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.445-16_445-15insGCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.403-16_403-15insGCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.307-16_307-15insGCTTTCC
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8410
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

12-53839777-C-CCTTTCCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839777
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839784
    reference: chr 12
allele count: 1
allele frequency: 8.479031355457952e-6
allele num: 117938
alternate allele: CCTTTCCT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.307-16_307-15insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.403-16_403-15insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.403-16_403-15insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.253-16_253-15insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.445-16_445-15insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*50-16_*50-15insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.115-16_115-15insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.253-16_253-15insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.403-16_403-15insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4556
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8410
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

12-53839784-C-CCTTTCCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839784
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839791
    reference: chr 12
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: CCTTTCCT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.253-9_253-8insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.115-9_115-8insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.307-9_307-8insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*50-9_*50-8insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.403-9_403-8insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.253-9_253-8insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.403-9_403-8insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.403-9_403-8insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.445-9_445-8insTCTTTCC
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7202
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5076
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

12-53839785-C-CTTTCCCG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839785
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839792
    reference: chr 12
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: CTTTCCCG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.307-8_307-7insGTTTCCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.253-8_253-7insGTTTCCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.403-8_403-7insGTTTCCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.253-8_253-7insGTTTCCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*50-8_*50-7insGTTTCCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.403-8_403-7insGTTTCCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.115-8_115-7insGTTTCCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.445-8_445-7insGTTTCCC
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.403-8_403-7insGTTTCCC
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5089
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4696
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7204
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5077
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-53839791-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839791
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839791
    reference: chr 12
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.403-8C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.253-8C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+2234C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+2234C>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*50-8C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.307-8C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.403-8C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.403-8C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.253-8C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.115-8C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.445-8C>T
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5099
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3596
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7200
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.403-8C>T
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

12-53839792-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839792
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839792
    reference: chr 12
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.403-7C>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.253-7C>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.253-7C>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+2235C>G
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+2235C>G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*50-7C>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.403-7C>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.403-7C>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.307-7C>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.445-7C>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.115-7C>G
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3596
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5099
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7199
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.403-7C>G
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

12-53839793-T-TTTCCCCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839793
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839800
    reference: chr 12
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: TTTCCCCC
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.403-5_403-4insTCCCCCT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.253-5_253-4insTCCCCCT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.445-5_445-4insTCCCCCT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.403-5_403-4insTCCCCCT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.307-5_307-4insTCCCCCT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.253-5_253-4insTCCCCCT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.403-5_403-4insTCCCCCT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.115-5_115-4insTCCCCCT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*50-5_*50-4insTCCCCCT
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  variant of: http://identifiers.org/hgnc/8648
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5099
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7199
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4196
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.403-5_403-4insTCCCCCT
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-53839795-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839795
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839795
    reference: chr 12
allele count: 1
allele frequency: 8.34752412434472e-6
allele num: 119796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*50-4G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+2238G>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.253-4G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.307-4G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.445-4G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.253-4G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+2238G>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.115-4G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.403-4G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.403-4G>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.403-4G>T
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7175
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4708
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4197
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.403-4G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

12-53839801-TTCCTCCTCTTCC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839801
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839789
    reference: chr 12
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsp: ENSP00000446818.1:p.Ser156_Ser159del
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsp: ENSP00000369112.4:p.Ser92_Ser95del
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsp: ENSP00000412064.2:p.Ser142_Ser145del
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsp: ENSP00000448761.1:p.Ser142_Ser145del
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsp: ENSP00000447777.1:p.Ser142_Ser145del
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsp: ENSP00000450334.1:p.Ser46_Ser49del
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsp: ENSP00000448153.1:p.Ser92_Ser95del
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsp: ENSP00000448481.1:p.Ser110_Ser113del
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4980
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4710
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1120
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser142_Ser145del
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: TTCCTCCTCTTCC
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

12-53839807-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839807
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839807
    reference: chr 12
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.411C>T
  hgvsp: ENST00000549135.1:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+2250C>T
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+2250C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.453C>T
  hgvsp: ENST00000547368.1:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.261C>T
  hgvsp: ENST00000549581.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.123C>T
  hgvsp: ENST00000546581.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.315C>T
  hgvsp: ENST00000551003.1:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.261C>T
  hgvsp: ENST00000379786.4:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.411C>T
  hgvsp: ENST00000549924.1:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*58C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.411C>T
  hgvsp: ENST00000429243.2:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5096
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6918
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser137Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

12-53839810-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839810
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839810
    reference: chr 12
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.126T>C
  hgvsp: ENST00000546581.1:c.126T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.264T>C
  hgvsp: ENST00000549581.1:c.264T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.318T>C
  hgvsp: ENST00000551003.1:c.318T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.264T>C
  hgvsp: ENST00000379786.4:c.264T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+2253T>C
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.414T>C
  hgvsp: ENST00000549924.1:c.414T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.456T>C
  hgvsp: ENST00000547368.1:c.456T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.414T>C
  hgvsp: ENST00000549135.1:c.414T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+2253T>C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.414T>C
  hgvsp: ENST00000429243.2:c.414T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*61T>C
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5097
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6916
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser138Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

12-53839812-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839812
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839812
    reference: chr 12
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.320C>T
  hgvsp: ENSP00000448481.1:p.Ser107Phe
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+2255C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.416C>T
  hgvsp: ENSP00000447777.1:p.Ser139Phe
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.458C>T
  hgvsp: ENSP00000446818.1:p.Ser153Phe
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*63C>T
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.128C>T
  hgvsp: ENSP00000450334.1:p.Ser43Phe
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.266C>T
  hgvsp: ENSP00000369112.4:p.Ser89Phe
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.416C>T
  hgvsp: ENSP00000448761.1:p.Ser139Phe
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.266C>T
  hgvsp: ENSP00000448153.1:p.Ser89Phe
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.416C>T
  hgvsp: ENSP00000412064.2:p.Ser139Phe
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+2255C>T
  variant of: http://identifiers.org/hgnc/8648
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6916
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3755
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser139Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-53839826-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53839826
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 53839826
    reference: chr 12
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197111
  ensembl protein: ENSP00000446130
  ensembl transcript: ENST00000541275
  gene symbol: PCBP2
  hgvsc: ENST00000541275.1:c.-76+2269A>G
  variant of: http://identifiers.org/hgnc/8648
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000446818
  ensembl transcript: ENST00000547368
  gene symbol: PRR13
  hgvsc: ENST00000547368.1:c.472A>G
  hgvsp: ENSP00000446818.1:p.Ser158Gly
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000447777
  ensembl transcript: ENST00000549135
  gene symbol: PRR13
  hgvsc: ENST00000549135.1:c.430A>G
  hgvsp: ENSP00000447777.1:p.Ser144Gly
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000449513
  ensembl transcript: ENST00000549068
  gene symbol: PRR13
  hgvsc: ENST00000549068.1:c.*77A>G
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000450334
  ensembl transcript: ENST00000546581
  gene symbol: PRR13
  hgvsc: ENST00000546581.1:c.142A>G
  hgvsp: ENSP00000450334.1:p.Ser48Gly
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448761
  ensembl transcript: ENST00000549924
  gene symbol: PRR13
  hgvsc: ENST00000549924.1:c.430A>G
  hgvsp: ENSP00000448761.1:p.Ser144Gly
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257379
  ensembl transcript: ENST00000547717
  gene symbol: RP11-793H13.8
  hgvsc: ENST00000547717.1:n.474+2269A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000369112
  ensembl transcript: ENST00000379786
  gene symbol: PRR13
  hgvsc: ENST00000379786.4:c.280A>G
  hgvsp: ENSP00000369112.4:p.Ser94Gly
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448481
  ensembl transcript: ENST00000551003
  gene symbol: PRR13
  hgvsc: ENST00000551003.1:c.334A>G
  hgvsp: ENSP00000448481.1:p.Ser112Gly
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000448153
  ensembl transcript: ENST00000549581
  gene symbol: PRR13
  hgvsc: ENST00000549581.1:c.280A>G
  hgvsp: ENSP00000448153.1:p.Ser94Gly
  variant of: http://identifiers.org/hgnc/24528
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000205352
  ensembl protein: ENSP00000412064
  ensembl transcript: ENST00000429243
  gene symbol: PRR13
  hgvsc: ENST00000429243.2:c.430A>G
  hgvsp: ENSP00000412064.2:p.Ser144Gly
  variant of: http://identifiers.org/hgnc/24528
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6914
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5096
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser144Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

GenotypeDepth
all individuals: 41
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 62
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3612
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 819
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10209
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35651
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 542
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 431
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2167
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1970
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2232
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 2.006880733944954e-3
allele num: 3488
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 910
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.374e0

VQSLOD
type: SiteQuality
SIO_000300: -5.543e0

MQRankSum
type: SiteQuality
SIO_000300: 3.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 5.18547e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.181e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.39e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

QD
type: SiteQuality
SIO_000300: 8.32e0

MQ
type: SiteQuality
SIO_000300: 2.652e1

GenotypeDepth
all individuals: 89
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 281
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3851
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2276
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1726
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 515
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9571
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35565
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2110
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1286
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3882
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1012
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13322
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

QD
type: SiteQuality
SIO_000300: 7.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQ
type: SiteQuality
SIO_000300: 2.679e1

VQSLOD
type: SiteQuality
SIO_000300: -5.096e0

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.30832e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.27e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeDepth
all individuals: 45
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 282
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4258
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8470
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 892
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2539
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2392
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1853
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1206
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35100
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.55307994757536e-5
allele num: 15260
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1196
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.625e0

QD
type: SiteQuality
SIO_000300: 8.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.03e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.165e0

FS
type: SiteQuality
SIO_000300: 7.83e0

MQ
type: SiteQuality
SIO_000300: 2.663e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.457e0

DP
type: SiteQuality
SIO_000300: 5.56466e5

GenotypeDepth
all individuals: 284
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 643
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33807
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1004
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2501
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2823
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2631
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7963
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3976
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 125
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4960
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2876
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.579098067287044e-4
allele num: 2794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.2482836100362e-4
allele num: 16022
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1636
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 2.763e1

QD
type: SiteQuality
SIO_000300: 9.34e0

DP
type: SiteQuality
SIO_000300: 5.6971e5

VQSLOD
type: SiteQuality
SIO_000300: -5.385e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.383e0

FS
type: SiteQuality
SIO_000300: 7.938e0

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-2

GenotypeDepth
all individuals: 15
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variant carriers: 0

GenotypeDepth
all individuals: 12
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variant carriers: 0

GenotypeDepth
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 518
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6604
bin: 6.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.914487910359741e-5
allele num: 20348
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1776
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3556
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.61e0

QD
type: SiteQuality
SIO_000300: 6.99e0

MQ
type: SiteQuality
SIO_000300: 3.014e1

VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

DP
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SIO_000300: 6.35876e5

FS
type: SiteQuality
SIO_000300: 2.363e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.62e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 689
bin: 4.25e1
variant carriers: 0

South Asian
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allele count: 1
allele frequency: 1.048437827636821e-4
allele num: 9538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.781576160943881e-5
allele num: 26444
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3266
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2392
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.428e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

FS
type: SiteQuality
SIO_000300: 5.735e0

VQSLOD
type: SiteQuality
SIO_000300: -4.597e0

MQ
type: SiteQuality
SIO_000300: 3.16e1

DP
type: SiteQuality
SIO_000300: 7.39652e5

MQRankSum
type: SiteQuality
SIO_000300: -5.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.12e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

GenotypeDepth
all individuals: 13
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variant carriers: 0

GenotypeDepth
all individuals: 16
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variant carriers: 0

GenotypeDepth
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 647
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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: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 27

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 891
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GenotypeQuality
all individuals: 688
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4294
num of homozygotes: 0

South Asian
type: Population
allele count: 29
allele frequency: 2.912231371761398e-3
allele num: 9958
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4654
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3450
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27680
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

MQ
type: SiteQuality
SIO_000300: 2.697e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

BaseQRankSum
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SIO_000300: 2.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.194e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.12e-2

DP
type: SiteQuality
SIO_000300: 7.63327e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.4e-1

QD
type: SiteQuality
SIO_000300: 1.207e1

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 740
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GenotypeQuality
all individuals: 17912
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3234
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11874
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.884670859054982e-5
allele num: 34666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5502
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.88e0

MQ
type: SiteQuality
SIO_000300: 2.598e1

DP
type: SiteQuality
SIO_000300: 8.71046e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ReadPosRankSum
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-3

VQSLOD
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SIO_000300: -5.659e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.25e-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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5950
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3652
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 38756
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5550
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.916402786573781e-5
allele num: 12632
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.32607e5

InbreedingCoeff
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SIO_000300: -5.2e-3

MQ
type: SiteQuality
SIO_000300: 2.605e1

VQSLOD
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ReadPosRankSum
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SIO_000300: 1.63e0

ClippingRankSum
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SIO_000300: -1.291e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 8.26e-1

QD
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SIO_000300: 6.89e0

BaseQRankSum
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SIO_000300: 2.94e0

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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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47322
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 7424
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 7.268498328245384e-5
allele num: 13758
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.16e0

VQSLOD
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InbreedingCoeff
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DP
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QD
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ClippingRankSum
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BaseQRankSum
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FS
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 2.824e1

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5126
num of homozygotes: 0

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

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

Latino
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allele count: 1
allele frequency: 1.091464745688714e-4
allele num: 9162
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 54900
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14604
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

MQ
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FS
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SIO_000300: 2.692e0

MQRankSum
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SIO_000300: 1.29e0

ReadPosRankSum
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BaseQRankSum
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SIO_000300: 5.6e-2

ClippingRankSum
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VQSLOD
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DP
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SIO_000300: 1.197944e6

QD
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SIO_000300: 2.807e1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7592
num of homozygotes: 0

Latino
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allele frequency: 1.01461038961039e-4
allele num: 9856
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.730283420424266e-5
allele num: 57794
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14980
num of homozygotes: 0

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

QD
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SIO_000300: 1.211e1

InbreedingCoeff
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ReadPosRankSum
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MQ
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VQSLOD
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BaseQRankSum
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FS
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ClippingRankSum
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SIO_000300: 6.6e-1

MQRankSum
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SIO_000300: 3.12e-1

DP
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SIO_000300: 1.247186e6

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8140
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.644628642852444e-5
allele num: 60804
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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DP
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SIO_000300: 1.302343e6

MQ
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SIO_000300: 3.847e1

FS
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SIO_000300: 9.082000000000001e0

InbreedingCoeff
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SIO_000300: -2.2e-3

BaseQRankSum
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MQRankSum
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SIO_000300: -5.8e-1

ReadPosRankSum
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SIO_000300: -7.85e-1

QD
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ClippingRankSum
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SIO_000300: 8.91e-1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9158
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64142
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.148548942449582e-5
allele num: 16264
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.33e1

ReadPosRankSum
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SIO_000300: -5.33e-1

InbreedingCoeff
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SIO_000300: 1.2e-3

BaseQRankSum
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VQSLOD
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FS
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SIO_000300: 4.389e0

MQRankSum
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SIO_000300: -4.88e-1

DP
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SIO_000300: 1.371195e6

ClippingRankSum
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SIO_000300: 1.26e0

QD
type: SiteQuality
SIO_000300: 1.311e1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.553470452991984e-5
allele num: 64372
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16318
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

MQRankSum
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SIO_000300: -5.95e-1

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

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 9.279881217520415e-5
allele num: 64656
num of homozygotes: 0

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

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

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

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

Latino
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allele count: 0
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num of homozygotes: 0

MQRankSum
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ClippingRankSum
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FS
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MQ
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DP
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VQSLOD
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QD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 1

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

Latino
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num of homozygotes: 0

East Asian
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allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
allele num: 9632
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.537988311288834e-5
allele num: 65020
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.54e-1

ReadPosRankSum
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SIO_000300: 1.19e0

FS
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SIO_000300: 0.0e0

VQSLOD
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QD
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MQ
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SIO_000300: 3.931e1

InbreedingCoeff
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SIO_000300: 1.8e-3

MQRankSum
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SIO_000300: 2.71e0

DP
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SIO_000300: 1.39183e6

BaseQRankSum
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SIO_000300: -3.32e0

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: 61
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GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.697164724299878e-5
allele num: 11498
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8636
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: 9918
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.86e1

ReadPosRankSum
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FS
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SIO_000300: 1.598e0

VQSLOD
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MQRankSum
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SIO_000300: -1.8e-1

MQ
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SIO_000300: 4.364e1

ClippingRankSum
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SIO_000300: -1.517e0

BaseQRankSum
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SIO_000300: -2.803e0

DP
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SIO_000300: 1.400967e6

InbreedingCoeff
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SIO_000300: 2.5e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 25
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9952
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65618
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.695652173913044e-5
allele num: 11500
num of homozygotes: 0

Other
type: Population
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: 16452
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

FS
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SIO_000300: 1.598e0

MQRankSum
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SIO_000300: 9.0e-1

DP
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SIO_000300: 1.402154e6

MQ
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SIO_000300: 4.364e1

QD
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SIO_000300: 1.86e1

BaseQRankSum
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SIO_000300: -2.906e0

ReadPosRankSum
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SIO_000300: 1.05e0

VQSLOD
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SIO_000300: -1.573e0

ClippingRankSum
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SIO_000300: -1.26e0

GenotypeDepth
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variant carriers: 12

GenotypeDepth
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variant carriers: 9

GenotypeDepth
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variant carriers: 1

GenotypeQuality
all individuals: 915
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GenotypeQuality
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GenotypeQuality
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variant carriers: 139

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 59
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GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 33
allele frequency: 5.010628606134224e-3
allele num: 6586
num of homozygotes: 2

Other
type: Population
allele count: 4
allele frequency: 4.444444444444444e-3
allele num: 900
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: 2
allele frequency: 2.002002002002002e-4
allele num: 9990
num of homozygotes: 0

European (Non-Finnish)
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allele count: 85
allele frequency: 1.293720130285227e-3
allele num: 65702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

Latino
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allele count: 19
allele frequency: 1.652748782185108e-3
allele num: 11496
num of homozygotes: 1

MQ
type: SiteQuality
SIO_000300: 3.68e1

QD
type: SiteQuality
SIO_000300: 1.033e1

BaseQRankSum
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SIO_000300: -1.63e0

DP
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SIO_000300: 1.407968e6

MQRankSum
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SIO_000300: 1.2e-2

FS
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SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.31e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.729e0

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: 11496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9990
num of homozygotes: 0

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

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 900
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.044047365377005e-5
allele num: 65702
num of homozygotes: 0

South Asian
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allele count: 0
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allele num: 16452
num of homozygotes: 0

ReadPosRankSum
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SIO_000300: 6.55e-1

MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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QD
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ClippingRankSum
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MQ
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BaseQRankSum
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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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bin: 3.75e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 9
allele frequency: 1.366908660125756e-4
allele num: 65842
num of homozygotes: 0

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

Latino
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allele count: 0
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num of homozygotes: 0

ClippingRankSum
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VQSLOD
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QD
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ReadPosRankSum
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BaseQRankSum
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MQ
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DP
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MQRankSum
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InbreedingCoeff
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SIO_000300: 6.7e-3

FS
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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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European (Non-Finnish)
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allele count: 0
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num of homozygotes: 0

Latino
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Other
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European (Finnish)
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African
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South Asian
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East Asian
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QD
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MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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VQSLOD
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ClippingRankSum
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FS
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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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European (Non-Finnish)
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East Asian
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European (Finnish)
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Other
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Latino
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South Asian
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QD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQ
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DP
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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Other
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African
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South Asian
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MQRankSum
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MQ
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QD
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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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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European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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African
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Other
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South Asian
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ClippingRankSum
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FS
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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MQ
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QD
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MQRankSum
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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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South Asian
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allele frequency: 6.349206349206349e-5
allele num: 15750
num of homozygotes: 0

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

GenotypeQuality
all individuals: 930
bin: 3.75e1
variant carriers: 1

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 7900
num of homozygotes: 0

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

East Asian
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allele count: 2
allele frequency: 2.882675122513693e-4
allele num: 6938
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 5.02224135457024e-4
allele num: 13938
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 52372
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4944
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8390
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.427e1

DP
type: SiteQuality
SIO_000300: 1.084324e6

InbreedingCoeff
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SIO_000300: -3.3e-3

MQRankSum
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SIO_000300: 7.17e-1

VQSLOD
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SIO_000300: -1.422e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-2

FS
type: SiteQuality
SIO_000300: 9.56e0

QD
type: SiteQuality
SIO_000300: 2.97e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.093e0

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
all individuals: 1616
bin: 6.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4438
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.567889620570712e-4
allele num: 6378
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6980
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7914
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13298
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 48214
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.6e-1

DP
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SIO_000300: 9.99269e5

FS
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SIO_000300: 9.890000000000001e0

VQSLOD
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BaseQRankSum
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SIO_000300: -1.2e0

ClippingRankSum
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MQ
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SIO_000300: 5.277e1

InbreedingCoeff
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SIO_000300: -4.7e-3

ReadPosRankSum
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SIO_000300: -9.350000000000001e-1

QD
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SIO_000300: 3.51e0

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
all individuals: 184
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.381978993919292e-4
allele num: 7236
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5824
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5718
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3812
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 42404
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.61e-1

DP
type: SiteQuality
SIO_000300: 9.0003e5

VQSLOD
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SIO_000300: -1.437e0

FS
type: SiteQuality
SIO_000300: 1.0434e1

MQ
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SIO_000300: 5.041e1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.587e0

MQRankSum
type: SiteQuality
SIO_000300: 1.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1051
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GenotypeQuality
all individuals: 98
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3762
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.730702665282105e-4
allele num: 5778
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42128
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7200
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5702
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

MQ
type: SiteQuality
SIO_000300: 4.248e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.01e-1

BaseQRankSum
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SIO_000300: 3.02e0

ReadPosRankSum
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SIO_000300: -1.369e0

QD
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SIO_000300: 1.382e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.958e0

DP
type: SiteQuality
SIO_000300: 8.93881e5

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
all individuals: 998
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GenotypeQuality
all individuals: 215
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6786
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3414
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 7.572889057175312e-4
allele num: 5282
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 38854
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 8.471704506946798e-5
allele num: 11804
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.932740626207963e-4
allele num: 5174
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.88e0

ReadPosRankSum
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InbreedingCoeff
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MQ
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FS
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QD
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MQRankSum
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DP
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SIO_000300: 8.32816e5

BaseQRankSum
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SIO_000300: -2.166e0

ClippingRankSum
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SIO_000300: -2.16e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 1
allele frequency: 1.980982567353407e-4
allele num: 5048
num of homozygotes: 0

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

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

South Asian
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 1.305414860842776e-4
allele num: 38302
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
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SIO_000300: -1.11e-2

MQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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QD
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FS
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DP
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BaseQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.082044011588486e-5
allele num: 32446
num of homozygotes: 0

European (Finnish)
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South Asian
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Latino
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African
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ClippingRankSum
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SIO_000300: 5.55e-1

InbreedingCoeff
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MQRankSum
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QD
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FS
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MQ
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 49
bin: 9.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.727526618956188e-5
allele num: 11458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 640
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1458
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4930
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.81e-2

QD
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SIO_000300: 1.061e1

VQSLOD
type: SiteQuality
SIO_000300: -3.14e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.355e0

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

MQ
type: SiteQuality
SIO_000300: 5.178e1

DP
type: SiteQuality
SIO_000300: 4.0016e5

ClippingRankSum
type: SiteQuality
SIO_000300: -4.12e-1

GenotypeDepth
all individuals: 44
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1017
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2914
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.33186e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.344e1

QD
type: SiteQuality
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BaseQRankSum
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VQSLOD
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SIO_000300: 1.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.72e-2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 10028
bin: 2.25e1
variant carriers: 1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 1.068376068376068e-3
allele num: 2808
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7978
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3100
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.97e-2

MQ
type: SiteQuality
SIO_000300: 5.158e1

QD
type: SiteQuality
SIO_000300: 1.266e1

MQRankSum
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SIO_000300: 5.37e-1

BaseQRankSum
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SIO_000300: -1.755e0

FS
type: SiteQuality
SIO_000300: 2.144e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.37e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.5e-3

DP
type: SiteQuality
SIO_000300: 3.19888e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 5104
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 114
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2524
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1328
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 84
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.574803149606299e-4
allele num: 6350
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.113e0

DP
type: SiteQuality
SIO_000300: 2.58032e5

MQ
type: SiteQuality
SIO_000300: 5.862e1

QD
type: SiteQuality
SIO_000300: 1.052e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.01e0

VQSLOD
type: SiteQuality
SIO_000300: -1.911e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

GenotypeDepth
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 260
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variant carriers: 0

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

GenotypeQuality
all individuals: 78
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GenotypeQuality
all individuals: 1092
bin: 6.25e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 80
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5880
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2424
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.619e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.57e-2

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.35812e5

MQ
type: SiteQuality
SIO_000300: 5.203e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516162290011523e-5
allele num: 65956
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: 898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11218
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.816e1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.672e0

MQRankSum
type: SiteQuality
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BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 4.425735e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-2

QD
type: SiteQuality
SIO_000300: 3.089e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11046
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9048
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.523786304208698e-5
allele num: 65626
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.79e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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FS
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ReadPosRankSum
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MQRankSum
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MQ
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SIO_000300: 5.478e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11028
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8996
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.067626513741878e-4
allele num: 65566
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.443411e6

FS
type: SiteQuality
SIO_000300: 1.863e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.36e1

BaseQRankSum
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SIO_000300: -2.574e0

QD
type: SiteQuality
SIO_000300: 9.43e0

MQRankSum
type: SiteQuality
SIO_000300: -2.976e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

GenotypeQuality
all individuals: 246
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1445
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2070
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1806
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1818
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1854
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1624
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42898
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 209
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.535532215465881e-4
allele num: 65124
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10808
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8390
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.538935056940597e-4
allele num: 6498
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.0e0

FS
type: SiteQuality
SIO_000300: 2.999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.66e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.331e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

MQ
type: SiteQuality
SIO_000300: 5.597e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.9e-3

DP
type: SiteQuality
SIO_000300: 4.450558e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.17e0

VQSLOD
type: SiteQuality
SIO_000300: -1.105e0

GenotypeQuality
all individuals: 4288
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 305
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1527
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42237
bin: 9.75e1
variant carriers: 133

GenotypeQuality
all individuals: 1197
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2286
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1665
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1563
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1614
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1264
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 4.75e1
variant carriers: 1

African
type: Population
allele count: 3
allele frequency: 4.127682993946065e-4
allele num: 7268
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 11
allele frequency: 1.754385964912281e-3
allele num: 6270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 114
allele frequency: 1.805511561609123e-3
allele num: 63140
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15708
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.885815185403178e-4
allele num: 10194
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

MQ
type: SiteQuality
SIO_000300: 5.819e1

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

DP
type: SiteQuality
SIO_000300: 4.545583e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e-1

FS
type: SiteQuality
SIO_000300: 1.259e0

QD
type: SiteQuality
SIO_000300: 1.531e1

GenotypeQuality
all individuals: 1665
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42237
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1563
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4288
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 203
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1264
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1614
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2286
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1197
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.58378207158695e-5
allele num: 63140
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6270
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15708
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8212
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

DP
type: SiteQuality
SIO_000300: 4.545583e6

MQ
type: SiteQuality
SIO_000300: 5.819e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.1e0

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

FS
type: SiteQuality
SIO_000300: 1.259e0

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

QD
type: SiteQuality
SIO_000300: 1.531e1

GenotypeQuality
all individuals: 751
bin: 8.75e1
variant carriers: 100

GenotypeQuality
all individuals: 168
bin: 3.25e1
variant carriers: 86

GenotypeQuality
all individuals: 108
bin: 1.75e1
variant carriers: 63

GenotypeQuality
all individuals: 1232
bin: 6.25e1
variant carriers: 96

GenotypeQuality
all individuals: 1144
bin: 9.25e1
variant carriers: 105

GenotypeQuality
all individuals: 152
bin: 3.75e1
variant carriers: 85

GenotypeQuality
all individuals: 133
bin: 4.75e1
variant carriers: 85

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 47

GenotypeQuality
all individuals: 51964
bin: 9.75e1
variant carriers: 18757

GenotypeQuality
all individuals: 1045
bin: 8.25e1
variant carriers: 105

GenotypeQuality
all individuals: 148
bin: 2.25e1
variant carriers: 67

GenotypeQuality
all individuals: 121
bin: 5.75e1
variant carriers: 94

GenotypeQuality
all individuals: 593
bin: 2.5e0
variant carriers: 52

GenotypeQuality
all individuals: 118
bin: 1.25e1
variant carriers: 67

GenotypeQuality
all individuals: 942
bin: 7.75e1
variant carriers: 98

GenotypeQuality
all individuals: 124
bin: 5.25e1
variant carriers: 86

GenotypeQuality
all individuals: 137
bin: 2.75e1
variant carriers: 68

GenotypeQuality
all individuals: 902
bin: 6.75e1
variant carriers: 108

African
type: Population
allele count: 4621
allele frequency: 4.591613672496025e-1
allele num: 10064
num of homozygotes: 1093

Other
type: Population
allele count: 156
allele frequency: 1.74496644295302e-1
allele num: 894
num of homozygotes: 12

Latino
type: Population
allele count: 2899
allele frequency: 2.55238598344779e-1
allele num: 11358
num of homozygotes: 277

European (Finnish)
type: Population
allele count: 921
allele frequency: 1.406106870229008e-1
allele num: 6550
num of homozygotes: 63

East Asian
type: Population
allele count: 1501
allele frequency: 1.744132000929584e-1
allele num: 8606
num of homozygotes: 98

European (Non-Finnish)
type: Population
allele count: 10305
allele frequency: 1.566966729517669e-1
allele num: 65764
num of homozygotes: 659

South Asian
type: Population
allele count: 2059
allele frequency: 1.269733596447953e-1
allele num: 16216
num of homozygotes: 157

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.13e-1

DP
type: SiteQuality
SIO_000300: 4.346891e6

MQ
type: SiteQuality
SIO_000300: 5.449e1

VQSLOD
type: SiteQuality
SIO_000300: -3.363e-1

QD
type: SiteQuality
SIO_000300: 6.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.36e-2

FS
type: SiteQuality
SIO_000300: 8.262e0

MQRankSum
type: SiteQuality
SIO_000300: -4.219e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.74e-1

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1232
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 751
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51964
bin: 9.75e1
variant carriers: 402

GenotypeQuality
all individuals: 902
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 942
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 118
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1144
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 11
allele frequency: 9.684803662616658e-4
allele num: 11358
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 30
allele frequency: 4.580152671755725e-3
allele num: 6550
num of homozygotes: 0

South Asian
type: Population
allele count: 27
allele frequency: 1.665022200296004e-3
allele num: 16216
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.968203497615262e-4
allele num: 10064
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 329
allele frequency: 5.00273705978955e-3
allele num: 65764
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16198001394376e-4
allele num: 8606
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.74e-1

QD
type: SiteQuality
SIO_000300: 6.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.36e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.363e-1

MQ
type: SiteQuality
SIO_000300: 5.449e1

FS
type: SiteQuality
SIO_000300: 8.262e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.13e-1

DP
type: SiteQuality
SIO_000300: 4.346891e6

MQRankSum
type: SiteQuality
SIO_000300: -4.219e0

GenotypeQuality
all individuals: 108
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51964
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 152
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 942
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1232
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11358
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65764
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16198001394376e-4
allele num: 8606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.262e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

MQ
type: SiteQuality
SIO_000300: 5.449e1

VQSLOD
type: SiteQuality
SIO_000300: -3.363e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.36e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.74e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.219e0

DP
type: SiteQuality
SIO_000300: 4.346891e6

QD
type: SiteQuality
SIO_000300: 6.07e0

GenotypeQuality
all individuals: 247
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1428
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 130
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1732
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1815
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1095
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1437
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48494
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1568
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 7
allele frequency: 7.185382878259084e-4
allele num: 9742
num of homozygotes: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16248
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.504672897196261e-4
allele num: 8560
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.869966294128082e-5
allele num: 11274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.221933710096227e-4
allele num: 65470
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.79e0

MQ
type: SiteQuality
SIO_000300: 5.377e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-2

QD
type: SiteQuality
SIO_000300: 6.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.627e0

FS
type: SiteQuality
SIO_000300: 8.262e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.444e-1

DP
type: SiteQuality
SIO_000300: 4.145149e6

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

GenotypeQuality
all individuals: 216
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1672
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 942
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1377
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 101
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 280
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 310
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1847
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 48526
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 1505
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 10
allele frequency: 1.051082615093546e-3
allele num: 9514
num of homozygotes: 4

East Asian
type: Population
allele count: 3
allele frequency: 3.50385423966363e-4
allele num: 8562
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.837222120154327e-4
allele num: 65316
num of homozygotes: 1

Latino
type: Population
allele count: 2
allele frequency: 1.784439685938615e-4
allele num: 11208
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16252
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.81e-1

QD
type: SiteQuality
SIO_000300: 1.183e1

VQSLOD
type: SiteQuality
SIO_000300: 2.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.38e-1

FS
type: SiteQuality
SIO_000300: 8.262e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.75e-1

DP
type: SiteQuality
SIO_000300: 4.175515e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.869e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.49e-1

MQ
type: SiteQuality
SIO_000300: 5.883e1

GenotypeQuality
all individuals: 120
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1345
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48485
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1500
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1373
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1874
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9408
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.97021887334051e-5
allele num: 11148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65250
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.564e1

QD
type: SiteQuality
SIO_000300: 4.4e0

FS
type: SiteQuality
SIO_000300: 8.247999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

VQSLOD
type: SiteQuality
SIO_000300: -5.957e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.258e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.45e-1

DP
type: SiteQuality
SIO_000300: 4.189657e6

GenotypeQuality
all individuals: 331
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1874
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1373
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 28

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 930
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1345
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48485
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1648
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11148
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65250
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.062925170068027e-4
allele num: 9408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.258e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.46e-1

FS
type: SiteQuality
SIO_000300: 8.247999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.45e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.957e-1

MQ
type: SiteQuality
SIO_000300: 5.564e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.45e-1

QD
type: SiteQuality
SIO_000300: 4.4e0

DP
type: SiteQuality
SIO_000300: 4.189657e6

GenotypeQuality
all individuals: 1099
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2503
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1814
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

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

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2032
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48531
bin: 9.75e1
variant carriers: 1

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

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.259e1

MQRankSum
type: SiteQuality
SIO_000300: -5.558e0

QD
type: SiteQuality
SIO_000300: 5.62e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.850000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.472e0

DP
type: SiteQuality
SIO_000300: 4.052795e6

GenotypeQuality
all individuals: 2513
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 2032
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variant carriers: 0

GenotypeQuality
all individuals: 48533
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1738
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variant carriers: 0

GenotypeQuality
all individuals: 1689
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

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

African
type: Population
allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.053039e6

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

QD
type: SiteQuality
SIO_000300: 5.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.113e0

MQRankSum
type: SiteQuality
SIO_000300: -2.199e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.870000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.26e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.52e-1

GenotypeDepth
all individuals: 1635
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1745
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1812
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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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variant carriers: 0

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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variant carriers: 1

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1224
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GenotypeQuality
all individuals: 2029
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.61e1

FS
type: SiteQuality
SIO_000300: 8.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

DP
type: SiteQuality
SIO_000300: 4.052796e6

MQRankSum
type: SiteQuality
SIO_000300: 3.21e0

VQSLOD
type: SiteQuality
SIO_000300: -2.07e0

MQ
type: SiteQuality
SIO_000300: 5.5e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.609e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.164e0

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2555
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 9.25e1
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: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

VQSLOD
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ClippingRankSum
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QD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.052563e6

FS
type: SiteQuality
SIO_000300: 6.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.28e-1

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.578e1

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: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2555
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GenotypeQuality
all individuals: 1100
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997152704930316e-5
allele num: 66730
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.191e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-2

FS
type: SiteQuality
SIO_000300: 9.125e0

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

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele frequency: 1.511258878645912e-5
allele num: 66170
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 908
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.4983967155144e-5
allele num: 66738
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FS
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SIO_000300: 3.0826e1

VQSLOD
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DP
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MQRankSum
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MQ
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SIO_000300: 5.279e1

BaseQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -2.38e-1

GenotypeQuality
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variant carriers: 1

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

East Asian
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allele frequency: 0.0e0
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Latino
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African
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South Asian
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European (Non-Finnish)
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allele num: 66730
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Other
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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MQ
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FS
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VQSLOD
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

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

East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

East Asian
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allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

Other
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European (Finnish)
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ReadPosRankSum
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FS
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DP
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InbreedingCoeff
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VQSLOD
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QD
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MQRankSum
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MQ
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ClippingRankSum
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