16-14721996-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14721996
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14721996
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 118048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.303+33C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.249+33C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.158+52C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-7+33C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.177+33C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.177+33C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.177+33C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.177+33C>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1652
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1388
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1607
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 852
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

16-14721996-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14721996
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14721996
    reference: chr 16
allele count: 1
allele frequency: 8.471130387638926e-6
allele num: 118048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.177+33C>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.158+52C>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-7+33C>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.177+33C>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.177+33C>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.249+33C>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.303+33C>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.177+33C>A
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23220
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1657
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5711
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1388
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

16-14722001-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722001
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722001
    reference: chr 16
allele count: 1
allele frequency: 8.438391305081599e-6
allele num: 118506
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.177+28T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.303+28T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-7+28T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.177+28T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.158+47T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.177+28T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.177+28T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.249+28T>C
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25105
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40117
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1606
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5825
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/16-14722003-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722003
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722003
    reference: chr 16
allele count: 2
allele frequency: 1.684919966301601e-5
allele num: 118700
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.303+26T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.177+26T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.177+26T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.177+26T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.158+45T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.249+26T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.177+26T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-7+26T>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17128
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40868
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3862
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

16-14722012-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722012
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722012
    reference: chr 16
allele count: 1
allele frequency: 8.36050497450046e-6
allele num: 119610
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.177+17G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.158+36G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-7+17G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.249+17G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.177+17G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.177+17G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.303+17G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.177+17G>A
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1587
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6009
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

16-14722013-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722013
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722013
    reference: chr 16
allele count: 6
allele frequency: 5.011610230367017e-5
allele num: 119722
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.158+35A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.177+16A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.177+16A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.249+16A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.177+16A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-7+16A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.303+16A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.177+16A>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26856
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7265
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6035
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1592
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3861
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 43293
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

16-14722030-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722030
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722030
    reference: chr 16
allele count: 1
allele frequency: 8.304682179812978e-6
allele num: 120414
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.176A>G
  hgvsp: ENSP00000445659.1:p.Lys59Arg
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.176A>G
  hgvsp: ENSP00000444381.1:p.Lys59Arg
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-8A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.302A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.248A>G
  hgvsp: ENSP00000456982.1:p.Lys83Arg
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.176A>G
  hgvsp: ENSP00000387911.2:p.Lys59Arg
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.176A>G
  hgvsp: ENSP00000458103.1:p.Lys59Arg
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.158+18A>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1063
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys59Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

16-14722037-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722037
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722037
    reference: chr 16
allele count: 1
allele frequency: 8.299443937256203e-6
allele num: 120490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.241C>T
  hgvsp: ENSP00000456982.1:p.Leu81Phe
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.158+11C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.169C>T
  hgvsp: ENSP00000444381.1:p.Leu57Phe
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-15C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.169C>T
  hgvsp: ENSP00000387911.2:p.Leu57Phe
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.169C>T
  hgvsp: ENSP00000445659.1:p.Leu57Phe
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.169C>T
  hgvsp: ENSP00000458103.1:p.Leu57Phe
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.295C>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44595
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6166
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu57Phe
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

16-14722038-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722038
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722038
    reference: chr 16
allele count: 1
allele frequency: 8.298755186721992e-6
allele num: 120500
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.168G>C
  hgvsp: ENSP00000445659.1:p.Lys56Asn
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.158+10G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.168G>C
  hgvsp: ENSP00000444381.1:p.Lys56Asn
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.240G>C
  hgvsp: ENSP00000456982.1:p.Lys80Asn
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.168G>C
  hgvsp: ENSP00000458103.1:p.Lys56Asn
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.168G>C
  hgvsp: ENSP00000387911.2:p.Lys56Asn
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.294G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-16G>C
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27145
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6166
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys56Asn
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

16-14722064-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722064
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722064
    reference: chr 16
allele count: 1
allele frequency: 8.293799555452344e-6
allele num: 120572
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-42G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.142G>C
  hgvsp: ENSP00000410525.2:p.Asp48His
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.142G>C
  hgvsp: ENSP00000387911.2:p.Asp48His
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.142G>C
  hgvsp: ENSP00000458103.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.142G>C
  hgvsp: ENSP00000445659.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.268G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.214G>C
  hgvsp: ENSP00000456982.1:p.Asp72His
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.142G>C
  hgvsp: ENSP00000444381.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp48His
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-14722064-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722064
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722064
    reference: chr 16
allele count: 1
allele frequency: 8.293799555452344e-6
allele num: 120572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.142G>A
  hgvsp: ENSP00000445659.1:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-42G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.142G>A
  hgvsp: ENSP00000444381.1:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.142G>A
  hgvsp: ENSP00000458103.1:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.214G>A
  hgvsp: ENSP00000456982.1:p.Asp72Asn
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.268G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.142G>A
  hgvsp: ENSP00000410525.2:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.142G>A
  hgvsp: ENSP00000387911.2:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1061
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp48Asn
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-14722070-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722070
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722070
    reference: chr 16
allele count: 3
allele frequency: 2.488511372496972e-5
allele num: 120554
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-48G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.262G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.136G>A
  hgvsp: ENSP00000458103.1:p.Gly46Ser
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.136G>A
  hgvsp: ENSP00000387911.2:p.Gly46Ser
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.136G>A
  hgvsp: ENSP00000410525.2:p.Gly46Ser
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.136G>A
  hgvsp: ENSP00000444381.1:p.Gly46Ser
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.136G>A
  hgvsp: ENSP00000445659.1:p.Gly46Ser
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.208G>A
  hgvsp: ENSP00000456982.1:p.Gly70Ser
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18724
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly46Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

16-14722071-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722071
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722071
    reference: chr 16
allele count: 1
allele frequency: 8.295175525914129e-6
allele num: 120552
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.135T>C
  hgvsp: ENST00000420015.2:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.207T>C
  hgvsp: ENST00000562896.1:c.207T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.135T>C
  hgvsp: ENST00000437198.2:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.261T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-49T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.135T>C
  hgvsp: ENST00000538472.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.135T>C
  hgvsp: ENST00000539279.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.135T>C
  hgvsp: ENST00000563641.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1062
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn45Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

16-14722073-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722073
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722073
    reference: chr 16
allele count: 1
allele frequency: 8.296138976920141e-6
allele num: 120538
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.133A>G
  hgvsp: ENSP00000387911.2:p.Asn45Asp
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.133A>G
  hgvsp: ENSP00000445659.1:p.Asn45Asp
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.205A>G
  hgvsp: ENSP00000456982.1:p.Asn69Asp
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.133A>G
  hgvsp: ENSP00000410525.2:p.Asn45Asp
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.133A>G
  hgvsp: ENSP00000458103.1:p.Asn45Asp
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.259A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.133A>G
  hgvsp: ENSP00000444381.1:p.Asn45Asp
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-51A>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44639
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3855
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asn45Asp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

16-14722073-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722073
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722073
    reference: chr 16
allele count: 1
allele frequency: 8.296138976920141e-6
allele num: 120538
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.205A>C
  hgvsp: ENSP00000456982.1:p.Asn69His
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.133A>C
  hgvsp: ENSP00000387911.2:p.Asn45His
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.133A>C
  hgvsp: ENSP00000445659.1:p.Asn45His
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.133A>C
  hgvsp: ENSP00000410525.2:p.Asn45His
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.133A>C
  hgvsp: ENSP00000458103.1:p.Asn45His
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-51A>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.133A>C
  hgvsp: ENSP00000444381.1:p.Asn45His
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.259A>C
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn45His
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

16-14722076-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722076
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722076
    reference: chr 16
allele count: 1
allele frequency: 8.298204268596276e-6
allele num: 120508
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.130A>G
  hgvsp: ENSP00000444381.1:p.Thr44Ala
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.130A>G
  hgvsp: ENSP00000387911.2:p.Thr44Ala
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.202A>G
  hgvsp: ENSP00000456982.1:p.Thr68Ala
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.130A>G
  hgvsp: ENSP00000445659.1:p.Thr44Ala
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.256A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.130A>G
  hgvsp: ENSP00000410525.2:p.Thr44Ala
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-54A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.130A>G
  hgvsp: ENSP00000458103.1:p.Thr44Ala
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18754
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3854
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr44Ala
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

16-14722088-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722088
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722088
    reference: chr 16
allele count: 1
allele frequency: 8.308408109006315e-6
allele num: 120360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.118G>A
  hgvsp: ENSP00000444381.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.118G>A
  hgvsp: ENSP00000387911.2:p.Val40Ile
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-66G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.190G>A
  hgvsp: ENSP00000456982.1:p.Val64Ile
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.118G>A
  hgvsp: ENSP00000458103.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.118G>A
  hgvsp: ENSP00000445659.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.118G>A
  hgvsp: ENSP00000410525.2:p.Val40Ile
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.244G>A
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26705
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44382
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val40Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP

16-14722112-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722112
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722112
    reference: chr 16
allele count: 1
allele frequency: 8.619500758516067e-6
allele num: 116016
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.98-4C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.170-4C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.98-4C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.98-4C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.224-4C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-86-4C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.98-4C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.98-4C>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17661
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1319
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3850
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
hgvs: c.98-4C>G
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-14722122-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722122
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722122
    reference: chr 16
allele count: 1
allele frequency: 8.908368521388993e-6
allele num: 112254
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.98-14T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.98-14T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.98-14T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.98-14T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.224-14T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.170-14T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.98-14T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-86-14T>C
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10991
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28403
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11170
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2356
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

16-14722130-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722130
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722130
    reference: chr 16
allele count: 17
allele frequency: 1.555295323135475e-4
allele num: 109304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.224-22A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.98-22A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.170-22A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.98-22A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.98-22A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-86-22A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.98-22A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.98-22A>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17471
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5585
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8366
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11743
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1118
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 1
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP

16-14722131-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722131
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722131
    reference: chr 16
allele count: 1
allele frequency: 9.179196269574637e-6
allele num: 108942
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.98-23A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.170-23A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.224-23A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.98-23A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.98-23A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-86-23A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.98-23A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.98-23A>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5401
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5017
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5503
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1114
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3784
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3846
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

16-14722136-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722136
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722136
    reference: chr 16
allele count: 5
allele frequency: 4.667923894168829e-5
allele num: 107114
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.98-28C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-86-28C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.98-28C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.98-28C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.224-28C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.98-28C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.98-28C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.170-28C>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19969
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5709
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5489
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8019
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3849
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6889
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3468
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1008
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

16-14722145-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722145
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722145
    reference: chr 16
allele count: 1
allele frequency: 9.770968498397562e-6
allele num: 102344
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.98-37A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.224-37A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.170-37A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.98-37A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.98-37A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-86-37A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.98-37A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.98-37A>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12338
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4147
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20009
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7360
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1965
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1022
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14953
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1855
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8078
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1769
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5820
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

16-14722149-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722149
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722149
    reference: chr 16
allele count: 3
allele frequency: 3.002041388143938e-5
allele num: 99932
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.224-41A>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.98-41A>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.98-41A>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.98-41A>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.98-41A>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-86-41A>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.170-41A>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.98-41A>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4309
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19022
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13298
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2365
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5632
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5114
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2779
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD

16-14722155-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722155
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722155
    reference: chr 16
allele count: 2
allele frequency: 2.093320215193318e-5
allele num: 95542
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.98-47G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-86-47G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.98-47G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.98-47G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.170-47G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.98-47G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.98-47G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.224-47G>A
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12973
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9950
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17869
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1060
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5060
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2128
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2543
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3031
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD

16-14722156-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14722156
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14722156
    reference: chr 16
allele count: 4
allele frequency: 4.182437943077019e-5
allele num: 95638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.224-48C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-86-48C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.98-48C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.98-48C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.98-48C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.170-48C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.98-48C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.98-48C>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17908
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12928
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9957
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1883
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3641
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6378
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2136
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5027
  bin: 2.75e1
  variant carriers: 0
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: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

16-14723406-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723406
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723406
    reference: chr 16
allele count: 2
allele frequency: 1.665306666222585e-5
allele num: 120098
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.97+48A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-87+48A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.223+48A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.169+48A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.97+48A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.97+48A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.97+48A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.97+48A>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5803
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8614
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11819
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16204
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1461
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3541
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

16-14723408-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723408
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723408
    reference: chr 16
allele count: 24
allele frequency: 1.998401278976818e-4
allele num: 120096
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-87+46C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.169+46C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.223+46C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.97+46C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.97+46C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.97+46C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.97+46C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.97+46C>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7980
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13018
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11880
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3685
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8609
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3518
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1191
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

16-14723410-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723410
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723410
    reference: chr 16
allele count: 2
allele frequency: 1.664752201634787e-5
allele num: 120138
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.97+44A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-87+44A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.97+44A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.97+44A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.97+44A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.169+44A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.97+44A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.223+44A>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5803
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8602
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/16-14723415-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723415
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723415
    reference: chr 16
allele count: 1
allele frequency: 8.321682977165302e-6
allele num: 120168
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.169+39T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.97+39T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.97+39T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.97+39T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.97+39T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.97+39T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.223+39T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-87+39T>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8609
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4662
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5170
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15330
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3547
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

16-14723425-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723425
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723425
    reference: chr 16
allele count: 24
allele frequency: 1.995078805612822e-4
allele num: 120296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.97+29C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.97+29C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.169+29C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.97+29C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.97+29C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.97+29C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.223+29C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-87+29C>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13827
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12223
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8624
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7047
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2381
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

16-14723432-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723432
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723432
    reference: chr 16
allele count: 1
allele frequency: 8.305096006909839e-6
allele num: 120408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.97+22A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.97+22A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.97+22A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-87+22A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.223+22A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.97+22A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.169+22A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.97+22A>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2390
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16807
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

16-14723432-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723432
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723432
    reference: chr 16
allele count: 4
allele frequency: 3.322038402763936e-5
allele num: 120408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.97+22A>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.223+22A>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.97+22A>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-87+22A>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.97+22A>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.97+22A>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.97+22A>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.169+22A>C
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7094
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16190
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

16-14723438-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723438
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723438
    reference: chr 16
allele count: 1
allele frequency: 8.302475798283047e-6
allele num: 120446
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.223+16A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.97+16A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.97+16A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.169+16A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.97+16A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.97+16A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.97+16A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-87+16A>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5815
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

16-14723440-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723440
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723440
    reference: chr 16
allele count: 1
allele frequency: 8.302475798283047e-6
allele num: 120446
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.97+14G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-87+14G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.223+14G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.97+14G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.97+14G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.169+14G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.97+14G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.97+14G>A
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5818
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12293
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16184
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4688
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3610
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-14723441-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723441
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723441
    reference: chr 16
allele count: 1
allele frequency: 8.301097405076952e-6
allele num: 120466
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.169+13T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.97+13T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.97+13T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.97+13T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-87+13T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.223+13T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.97+13T>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.97+13T>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5209
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17007
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

16-14723445-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723445
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723445
    reference: chr 16
allele count: 2
allele frequency: 1.659888787451241e-5
allele num: 120490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.97+9C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-87+9C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.97+9C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.97+9C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.169+9C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.223+9C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.97+9C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.97+9C>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3611
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17079
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

16-14723475-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723475
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723475
    reference: chr 16
allele count: 2
allele frequency: 1.65812731101494e-5
allele num: 120618
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.76G>A
  hgvsp: ENSP00000410525.2:p.Ala26Thr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.76G>A
  hgvsp: ENSP00000444381.1:p.Ala26Thr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.148G>A
  hgvsp: ENSP00000456982.1:p.Ala50Thr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.202G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-108G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.76G>A
  hgvsp: ENSP00000445659.1:p.Ala26Thr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.76G>A
  hgvsp: ENSP00000387911.2:p.Ala26Thr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.76G>A
  hgvsp: ENSP00000458103.1:p.Ala26Thr
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5813
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4695
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7153
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17310
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala26Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-14723476-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723476
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723476
    reference: chr 16
allele count: 1
allele frequency: 8.290361625574107e-6
allele num: 120622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.75C>T
  hgvsp: ENST00000539279.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.147C>T
  hgvsp: ENST00000562896.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-109C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.75C>T
  hgvsp: ENST00000437198.2:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.75C>T
  hgvsp: ENST00000538472.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.75C>T
  hgvsp: ENST00000563641.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.201C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.75C>T
  hgvsp: ENST00000420015.2:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7154
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16183
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3620
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe25Phe
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-14723479-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723479
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723479
    reference: chr 16
allele count: 1
allele frequency: 8.28953694646617e-6
allele num: 120634
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.72C>T
  hgvsp: ENST00000539279.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-112C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.72C>T
  hgvsp: ENST00000420015.2:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.72C>T
  hgvsp: ENST00000538472.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.144C>T
  hgvsp: ENST00000562896.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.72C>T
  hgvsp: ENST00000437198.2:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.72C>T
  hgvsp: ENST00000563641.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.198C>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14306
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10205
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2387
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Phe24Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

16-14723489-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723489
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723489
    reference: chr 16
allele count: 1
allele frequency: 8.288849839196314e-6
allele num: 120644
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.62A>G
  hgvsp: ENSP00000445659.1:p.Glu21Gly
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.134A>G
  hgvsp: ENSP00000456982.1:p.Glu45Gly
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.62A>G
  hgvsp: ENSP00000387911.2:p.Glu21Gly
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.62A>G
  hgvsp: ENSP00000410525.2:p.Glu21Gly
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.188A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.62A>G
  hgvsp: ENSP00000458103.1:p.Glu21Gly
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.62A>G
  hgvsp: ENSP00000444381.1:p.Glu21Gly
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-122A>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3611
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Glu21Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

16-14723495-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723495
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723495
    reference: chr 16
allele count: 1
allele frequency: 8.288437629506838e-6
allele num: 120650
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.128T>C
  hgvsp: ENSP00000456982.1:p.Ile43Thr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.56T>C
  hgvsp: ENSP00000458103.1:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.182T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.56T>C
  hgvsp: ENSP00000444381.1:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.56T>C
  hgvsp: ENSP00000445659.1:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-128T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.56T>C
  hgvsp: ENSP00000410525.2:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.56T>C
  hgvsp: ENSP00000387911.2:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17315
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3610
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile19Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD

16-14723496-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723496
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723496
    reference: chr 16
allele count: 3
allele frequency: 2.486531288852051e-5
allele num: 120650
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.55A>G
  hgvsp: ENSP00000445659.1:p.Ile19Val
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.127A>G
  hgvsp: ENSP00000456982.1:p.Ile43Val
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-129A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.55A>G
  hgvsp: ENSP00000410525.2:p.Ile19Val
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.55A>G
  hgvsp: ENSP00000387911.2:p.Ile19Val
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.181A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.55A>G
  hgvsp: ENSP00000458103.1:p.Ile19Val
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.55A>G
  hgvsp: ENSP00000444381.1:p.Ile19Val
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5220
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile19Val
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ

16-14723501-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723501
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723501
    reference: chr 16
allele count: 3
allele frequency: 2.486572508454347e-5
allele num: 120648
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.50A>G
  hgvsp: ENSP00000410525.2:p.Gln17Arg
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.50A>G
  hgvsp: ENSP00000445659.1:p.Gln17Arg
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.122A>G
  hgvsp: ENSP00000456982.1:p.Gln41Arg
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.50A>G
  hgvsp: ENSP00000444381.1:p.Gln17Arg
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-134A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.50A>G
  hgvsp: ENSP00000458103.1:p.Gln17Arg
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.176A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.50A>G
  hgvsp: ENSP00000387911.2:p.Gln17Arg
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17296
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2388
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5220
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16186
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Gln17Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP

16-14723503-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723503
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723503
    reference: chr 16
allele count: 3
allele frequency: 2.486654951758894e-5
allele num: 120644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.48C>T
  hgvsp: ENST00000539279.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.174C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-136C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.48C>T
  hgvsp: ENST00000563641.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.120C>T
  hgvsp: ENST00000562896.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.48C>T
  hgvsp: ENST00000538472.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.48C>T
  hgvsp: ENST00000420015.2:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.48C>T
  hgvsp: ENST00000437198.2:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Tyr16Tyr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

16-14723506-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723506
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723506
    reference: chr 16
allele count: 1
allele frequency: 8.288162845823595e-6
allele num: 120654
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.45G>A
  hgvsp: ENST00000420015.2:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.117G>A
  hgvsp: ENST00000562896.1:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.45G>A
  hgvsp: ENST00000437198.2:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.45G>A
  hgvsp: ENST00000539279.1:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.45G>A
  hgvsp: ENST00000538472.1:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-139G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.45G>A
  hgvsp: ENST00000563641.1:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.171G>A
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10170
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4699
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7156
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val15Val
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

16-14723508-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723508
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723508
    reference: chr 16
allele count: 1
allele frequency: 8.288575028181154e-6
allele num: 120648
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-141G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.43G>A
  hgvsp: ENSP00000387911.2:p.Val15Met
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.115G>A
  hgvsp: ENSP00000456982.1:p.Val39Met
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.43G>A
  hgvsp: ENSP00000445659.1:p.Val15Met
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.43G>A
  hgvsp: ENSP00000410525.2:p.Val15Met
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.43G>A
  hgvsp: ENSP00000458103.1:p.Val15Met
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.43G>A
  hgvsp: ENSP00000444381.1:p.Val15Met
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.169G>A
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5815
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4699
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7152
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val15Met
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-14723511-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723511
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723511
    reference: chr 16
allele count: 1
allele frequency: 8.288849839196314e-6
allele num: 120644
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.40A>G
  hgvsp: ENSP00000410525.2:p.Lys14Glu
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.40A>G
  hgvsp: ENSP00000458103.1:p.Lys14Glu
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.166A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.40A>G
  hgvsp: ENSP00000444381.1:p.Lys14Glu
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.112A>G
  hgvsp: ENSP00000456982.1:p.Lys38Glu
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.40A>G
  hgvsp: ENSP00000445659.1:p.Lys14Glu
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-144A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.40A>G
  hgvsp: ENSP00000387911.2:p.Lys14Glu
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2387
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3616
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5214
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17298
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys14Glu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

16-14723514-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723514
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723514
    reference: chr 16
allele count: 2
allele frequency: 1.657769967839263e-5
allele num: 120644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.37C>T
  hgvsp: ENSP00000444381.1:p.His13Tyr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.109C>T
  hgvsp: ENSP00000456982.1:p.His37Tyr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.37C>T
  hgvsp: ENSP00000445659.1:p.His13Tyr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.37C>T
  hgvsp: ENSP00000410525.2:p.His13Tyr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.37C>T
  hgvsp: ENSP00000458103.1:p.His13Tyr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-147C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.37C>T
  hgvsp: ENSP00000387911.2:p.His13Tyr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.163C>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3615
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7151
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4697
  bin: 8.25e1
  variant carriers: 0
hgvs: p.His13Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

16-14723517-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723517
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723517
    reference: chr 16
allele count: 1
allele frequency: 8.289124668435012e-6
allele num: 120640
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-150C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.34C>T
  hgvsp: ENSP00000410525.2:p.Leu12Phe
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.106C>T
  hgvsp: ENSP00000456982.1:p.Leu36Phe
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.34C>T
  hgvsp: ENSP00000387911.2:p.Leu12Phe
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.34C>T
  hgvsp: ENSP00000444381.1:p.Leu12Phe
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.34C>T
  hgvsp: ENSP00000458103.1:p.Leu12Phe
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.34C>T
  hgvsp: ENSP00000445659.1:p.Leu12Phe
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.160C>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17291
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7149
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu12Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-14723519-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723519
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723519
    reference: chr 16
allele count: 3
allele frequency: 2.48681985476972e-5
allele num: 120636
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.32A>G
  hgvsp: ENSP00000445659.1:p.Asn11Ser
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.32A>G
  hgvsp: ENSP00000410525.2:p.Asn11Ser
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.32A>G
  hgvsp: ENSP00000444381.1:p.Asn11Ser
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.32A>G
  hgvsp: ENSP00000458103.1:p.Asn11Ser
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.32A>G
  hgvsp: ENSP00000387911.2:p.Asn11Ser
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.104A>G
  hgvsp: ENSP00000456982.1:p.Asn35Ser
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-152A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.158A>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17276
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn11Ser
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

16-14723519-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723519
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723519
    reference: chr 16
allele count: 1
allele frequency: 8.289399515899069e-6
allele num: 120636
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.32A>C
  hgvsp: ENSP00000445659.1:p.Asn11Thr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.32A>C
  hgvsp: ENSP00000458103.1:p.Asn11Thr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.158A>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-152A>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.32A>C
  hgvsp: ENSP00000444381.1:p.Asn11Thr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.104A>C
  hgvsp: ENSP00000456982.1:p.Asn35Thr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.32A>C
  hgvsp: ENSP00000387911.2:p.Asn11Thr
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.32A>C
  hgvsp: ENSP00000410525.2:p.Asn11Thr
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3612
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn11Thr
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD

16-14723520-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723520
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723520
    reference: chr 16
allele count: 1
allele frequency: 8.289262089888757e-6
allele num: 120638
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.157A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.31A>G
  hgvsp: ENSP00000458103.1:p.Asn11Asp
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.31A>G
  hgvsp: ENSP00000387911.2:p.Asn11Asp
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.31A>G
  hgvsp: ENSP00000410525.2:p.Asn11Asp
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.31A>G
  hgvsp: ENSP00000445659.1:p.Asn11Asp
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.31A>G
  hgvsp: ENSP00000444381.1:p.Asn11Asp
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.103A>G
  hgvsp: ENSP00000456982.1:p.Asn35Asp
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-153A>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3612
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn11Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD

16-14723524-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723524
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723524
    reference: chr 16
allele count: 1
allele frequency: 8.28953694646617e-6
allele num: 120634
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.27G>A
  hgvsp: ENST00000538472.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.27G>A
  hgvsp: ENST00000563641.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.27G>A
  hgvsp: ENST00000420015.2:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.27G>A
  hgvsp: ENST00000437198.2:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.99G>A
  hgvsp: ENST00000562896.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.153G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-157G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.27G>A
  hgvsp: ENST00000539279.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16183
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3613
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys9Lys
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

16-14723536-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723536
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723536
    reference: chr 16
allele count: 2
allele frequency: 1.658484808279156e-5
allele num: 120592
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.20-5C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-164-5C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.20-5C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.20-5C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.20-5C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.20-5C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.92-5C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.146-5C>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3613
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3608
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7123
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.25e1
  variant carriers: 0
hgvs: c.20-5C>T
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

16-14723537-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723537
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723537
    reference: chr 16
allele count: 1
allele frequency: 8.29228651508367e-6
allele num: 120594
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.20-6C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-164-6C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.20-6C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.20-6C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.20-6C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.92-6C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.20-6C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.146-6C>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3613
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16182
  bin: 9.75e1
  variant carriers: 1
hgvs: c.20-6C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum

16-14723539-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723539
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723539
    reference: chr 16
allele count: 1
allele frequency: 8.293524416135881e-6
allele num: 120576
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.146-8C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.20-8C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.20-8C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.20-8C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.92-8C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-164-8C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.20-8C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.20-8C>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3613
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4690
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16183
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17042
  bin: 6.25e1
  variant carriers: 0
hgvs: c.20-8C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-14723539-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723539
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723539
    reference: chr 16
allele count: 1
allele frequency: 8.293524416135881e-6
allele num: 120576
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.92-8C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.20-8C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.20-8C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.20-8C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.20-8C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-164-8C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.20-8C>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.146-8C>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2389
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5211
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.25e1
  variant carriers: 0
hgvs: c.20-8C>G
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: G
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

16-14723539-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723539
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723539
    reference: chr 16
allele count: 1
allele frequency: 8.293524416135881e-6
allele num: 120576
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.92-8C>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.20-8C>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.20-8C>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-164-8C>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.20-8C>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.20-8C>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.146-8C>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.20-8C>A
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12318
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7122
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3606
  bin: 7.25e1
  variant carriers: 0
hgvs: c.20-8C>A
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

16-14723542-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723542
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723542
    reference: chr 16
allele count: 1
allele frequency: 8.294074713025015e-6
allele num: 120568
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.20-11T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.20-11T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.20-11T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.92-11T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.20-11T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.20-11T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.146-11T>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-164-11T>C
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5210
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

16-14723553-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723553
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723553
    reference: chr 16
allele count: 1
allele frequency: 8.29985724245543e-6
allele num: 120484
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.92-22C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.20-22C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.146-22C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.20-22C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.20-22C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.20-22C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-164-22C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.20-22C>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5817
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7064
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16179
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3590
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16407
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2386
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

16-14723561-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723561
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723561
    reference: chr 16
allele count: 6
allele frequency: 4.982892070557752e-5
allele num: 120412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.92-30G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.20-30G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.20-30G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-164-30G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.146-30G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.20-30G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.20-30G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.20-30G>C
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5818
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12236
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6948
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5184
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

16-14723562-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723562
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723562
    reference: chr 16
allele count: 2
allele frequency: 1.661046791688122e-5
allele num: 120406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.92-31G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.20-31G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.146-31G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.20-31G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.20-31G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.20-31G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-164-31G>C
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.20-31G>C
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2383
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5173
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

16-14723565-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723565
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723565
    reference: chr 16
allele count: 1
allele frequency: 8.305785810395521e-6
allele num: 120398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.20-34A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.20-34A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.20-34A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.92-34A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-164-34A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.20-34A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.20-34A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.146-34A>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2381
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

16-14723570-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723570
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723570
    reference: chr 16
allele count: 1
allele frequency: 8.311170212765958e-6
allele num: 120320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.20-39A>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.92-39A>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.20-39A>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.20-39A>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-164-39A>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.20-39A>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.20-39A>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.146-39A>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8625
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6491
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 888
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2376
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-14723575-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723575
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723575
    reference: chr 16
allele count: 150
allele frequency: 1.247007182761373e-3
allele num: 120288
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.92-44A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-164-44A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.20-44A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.146-44A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.20-44A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.20-44A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.20-44A>G
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.20-44A>G
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11607
  bin: 3.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12397
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 8905
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5809
  bin: 4.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 5.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 4.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8566
  bin: 3.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2371
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3589
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6239
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1611
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

16-14723919-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723919
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723919
    reference: chr 16
allele count: 1
allele frequency: 4.800307219662058e-5
allele num: 20832
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.19+45C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.19+45C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.19+45C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.92-388C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.145+45C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-165+128C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.19+45C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.19+45C>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15000
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4777
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4927
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1748
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2705
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24298
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD

16-14723923-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723923
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723923
    reference: chr 16
allele count: 1
allele frequency: 4.788813332056317e-5
allele num: 20882
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.19+41G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.92-392G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.19+41G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-165+124G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.19+41G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.19+41G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.19+41G>A
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.145+41G>A
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15221
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30167
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3239
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2933
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-14723924-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723924
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723924
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 20862
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.19+40G>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.19+40G>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.19+40G>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-165+123G>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.92-393G>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.145+40G>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.19+40G>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.19+40G>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15319
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25837
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2865
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

16-14723926-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723926
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723926
    reference: chr 16
allele count: 1
allele frequency: 4.793863854266539e-5
allele num: 20860
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.92-395C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.19+38C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.19+38C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-165+121C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.19+38C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.19+38C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.145+38C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.19+38C>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29974
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4069
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2821
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3331
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26056
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

16-14723927-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 14723927
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 14723927
    reference: chr 16
allele count: 5
allele frequency: 2.392573452004977e-4
allele num: 20898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000410525
  ensembl transcript: ENST00000420015
  gene symbol: PARN
  hgvsc: ENST00000420015.2:c.19+37C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000456982
  ensembl transcript: ENST00000562896
  gene symbol: PARN
  hgvsc: ENST00000562896.1:c.92-396C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000387911
  ensembl transcript: ENST00000437198
  gene symbol: PARN
  hgvsc: ENST00000437198.2:c.19+37C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl transcript: ENST00000566021
  gene symbol: PARN
  hgvsc: ENST00000566021.1:n.145+37C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000458103
  ensembl transcript: ENST00000563641
  gene symbol: PARN
  hgvsc: ENST00000563641.1:c.19+37C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000445659
  ensembl transcript: ENST00000538472
  gene symbol: PARN
  hgvsc: ENST00000538472.1:c.19+37C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000345456
  ensembl transcript: ENST00000341484
  gene symbol: PARN
  hgvsc: ENST00000341484.7:c.-165+120C>T
  variant of: http://identifiers.org/hgnc/8609
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140694
  ensembl protein: ENSP00000444381
  ensembl transcript: ENST00000539279
  gene symbol: PARN
  hgvsc: ENST00000539279.1:c.19+37C>T
  variant of: http://identifiers.org/hgnc/8609
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29907
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15604
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 763
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3859
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37018
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1657
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5711
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65128
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9644
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11246
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16300
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

DP
type: SiteQuality
SIO_000300: 1.591966e6

QD
type: SiteQuality
SIO_000300: 1.007e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e-1

GenotypeQuality
all individuals: 54
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.134969325153375e-5
allele num: 16300
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65128
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9644
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.591966e6

QD
type: SiteQuality
SIO_000300: 1.007e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

GenotypeQuality
all individuals: 931
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8338
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11310
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.120700208103807e-5
allele num: 16338
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65392
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.696e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e0

MQRankSum
type: SiteQuality
SIO_000300: 8.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.336e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

DP
type: SiteQuality
SIO_000300: 1.615643e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.25e0

GenotypeQuality
all individuals: 200
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1610
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11330
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 2.069108214359611e-4
allele num: 9666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8364
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65510
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.622323e6

MQRankSum
type: SiteQuality
SIO_000300: -4.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

FS
type: SiteQuality
SIO_000300: 4.067e0

VQSLOD
type: SiteQuality
SIO_000300: -9.206e-1

MQ
type: SiteQuality
SIO_000300: 5.906e1

QD
type: SiteQuality
SIO_000300: 1.748e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.03e-1

GenotypeQuality
all individuals: 792
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
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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
all individuals: 10
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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
all individuals: 1068
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variant carriers: 0

GenotypeQuality
all individuals: 3856
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9714
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66074
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.098304671301378e-5
allele num: 16398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.646455e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 9.630000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: -6.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.44e-1

FS
type: SiteQuality
SIO_000300: 3.041e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.982e0

VQSLOD
type: SiteQuality
SIO_000300: 4.8e-1

GenotypeQuality
all individuals: 171
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 790
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variant carriers: 0

GenotypeQuality
all individuals: 323
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variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 530
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variant carriers: 0

GenotypeQuality
all individuals: 1402
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
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variant carriers: 0

GenotypeQuality
all individuals: 1071
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variant carriers: 0

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

East Asian
type: Population
allele count: 6
allele frequency: 7.038948850305022e-4
allele num: 8524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9720
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66142
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.662e0

QD
type: SiteQuality
SIO_000300: 1.226e1

VQSLOD
type: SiteQuality
SIO_000300: 9.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.64878e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.51e-1

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1603
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variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 74
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variant carriers: 0

GenotypeQuality
all individuals: 75
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 44353
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 788
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.071645415907711e-5
allele num: 16470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66554
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9764
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: 8596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.152e0

MQRankSum
type: SiteQuality
SIO_000300: -4.89e-1

DP
type: SiteQuality
SIO_000300: 1.664809e6

VQSLOD
type: SiteQuality
SIO_000300: -3.118e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.912e1

QD
type: SiteQuality
SIO_000300: 1.146e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.97e-1

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
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variant carriers: 0

GenotypeQuality
all individuals: 152
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GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 789
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1066
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GenotypeQuality
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GenotypeQuality
all individuals: 37
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1414
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1601
bin: 7.75e1
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GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.023751023751024e-4
allele num: 9768
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.819e0

QD
type: SiteQuality
SIO_000300: 8.609999999999999e0

FS
type: SiteQuality
SIO_000300: 4.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

DP
type: SiteQuality
SIO_000300: 1.666278e6

MQRankSum
type: SiteQuality
SIO_000300: -3.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
all individuals: 3856
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variant carriers: 1

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 153
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GenotypeQuality
all individuals: 46
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GenotypeQuality
all individuals: 18
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GenotypeQuality
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GenotypeQuality
all individuals: 1413
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1602
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501411326647048e-5
allele num: 66604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.666581e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.9e-1

QD
type: SiteQuality
SIO_000300: 1.134e1

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

FS
type: SiteQuality
SIO_000300: 5.287e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

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

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1061
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 136
bin: 2.25e1
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GenotypeQuality
all individuals: 1600
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 6187
bin: 6.75e1
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GenotypeQuality
all individuals: 44691
bin: 6.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.022704029453876e-4
allele num: 9778
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

DP
type: SiteQuality
SIO_000300: 1.66862e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.28e-1

QD
type: SiteQuality
SIO_000300: 9.57e0

FS
type: SiteQuality
SIO_000300: 3.924e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.320000000000001e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3855
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 6.066488716330988e-5
allele num: 16484
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
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: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.924e0

MQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.28e-1

QD
type: SiteQuality
SIO_000300: 9.57e0

DP
type: SiteQuality
SIO_000300: 1.66862e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.320000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66628
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9774
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.481894150417827e-4
allele num: 8616
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.9e-2

DP
type: SiteQuality
SIO_000300: 1.668388e6

QD
type: SiteQuality
SIO_000300: 1.012e1

FS
type: SiteQuality
SIO_000300: 2.145e0

VQSLOD
type: SiteQuality
SIO_000300: 1.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

MQ
type: SiteQuality
SIO_000300: 5.921e1

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9774
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.381e0

DP
type: SiteQuality
SIO_000300: 1.668152e6

MQ
type: SiteQuality
SIO_000300: 5.638e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.16e-1

FS
type: SiteQuality
SIO_000300: 1.083e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.862e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

QD
type: SiteQuality
SIO_000300: 1.056e1

VQSLOD
type: SiteQuality
SIO_000300: -9.295e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.665511265164645e-5
allele num: 11540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.19e-1

MQ
type: SiteQuality
SIO_000300: 5.92e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 6.867e0

DP
type: SiteQuality
SIO_000300: 1.668088e6

VQSLOD
type: SiteQuality
SIO_000300: -9.23e-1

QD
type: SiteQuality
SIO_000300: 1.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 526
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160631383472609e-4
allele num: 8616
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.74e0

FS
type: SiteQuality
SIO_000300: 6.867e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.668088e6

VQSLOD
type: SiteQuality
SIO_000300: -9.23e-1

QD
type: SiteQuality
SIO_000300: 1.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.19e-1

MQ
type: SiteQuality
SIO_000300: 5.92e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

GenotypeQuality
all individuals: 44603
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1061
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.023960679909891e-4
allele num: 9766
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: 11534
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.78e0

VQSLOD
type: SiteQuality
SIO_000300: 2.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.01e-1

DP
type: SiteQuality
SIO_000300: 1.667796e6

MQ
type: SiteQuality
SIO_000300: 5.936e1

QD
type: SiteQuality
SIO_000300: 1.53e1

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 2.25e1
variant carriers: 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: 8610
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9754
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503714174009804e-5
allele num: 66502
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.59e-1

FS
type: SiteQuality
SIO_000300: 5.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e0

MQRankSum
type: SiteQuality
SIO_000300: -2.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.398e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.543e1

DP
type: SiteQuality
SIO_000300: 1.665668e6

GenotypeQuality
all individuals: 1510
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 519
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variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11044
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.56563126252505e-5
allele num: 63872
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16078
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8228
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9440
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.887e1

FS
type: SiteQuality
SIO_000300: 5.724e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 311
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7876
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6316
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.396729937981582e-5
allele num: 10642
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61538
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.953e1

MQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

FS
type: SiteQuality
SIO_000300: 4.723e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

DP
type: SiteQuality
SIO_000300: 1.461872e6

VQSLOD
type: SiteQuality
SIO_000300: -9.823e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 4073
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 779
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2329
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3859
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 14821
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18728
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5032
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1014
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3867
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1393
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 4
allele frequency: 4.440497335701599e-4
allele num: 9008
num of homozygotes: 1

Latino
type: Population
allele count: 1
allele frequency: 9.723842862699339e-5
allele num: 10284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.83878840560329e-4
allele num: 59822
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.608234158893535e-4
allele num: 6218
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

QD
type: SiteQuality
SIO_000300: 1.68e1

VQSLOD
type: SiteQuality
SIO_000300: 6.870000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.18e-1

FS
type: SiteQuality
SIO_000300: 3.488e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.333919e6

GenotypeQuality
all individuals: 815
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5431
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15064
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variant carriers: 0

GenotypeQuality
all individuals: 4305
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2598
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1393
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1012
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10254
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.11333778668448e-4
allele num: 8982
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59568
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7518
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0288e1

DP
type: SiteQuality
SIO_000300: 1.315958e6

QD
type: SiteQuality
SIO_000300: 1.505e1

MQRankSum
type: SiteQuality
SIO_000300: -9.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.119e-1

GenotypeQuality
all individuals: 778
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15330
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 736
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1374
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3813
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12722
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6126
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.196172248803828e-3
allele num: 836
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8842
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.299207483435105e-4
allele num: 15394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7390
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.994415636218588e-4
allele num: 10028
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.511e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

DP
type: SiteQuality
SIO_000300: 1.253917e6

VQSLOD
type: SiteQuality
SIO_000300: 3.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.512e0

MQRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.245e1

GenotypeQuality
all individuals: 1837
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1085
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 504
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variant carriers: 0

GenotypeQuality
all individuals: 8080
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5071
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3839
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5924
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.799143607642762e-5
allele num: 55582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7006
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14966
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.214e0

MQRankSum
type: SiteQuality
SIO_000300: -5.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.871e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.117e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

DP
type: SiteQuality
SIO_000300: 1.157754e6

GenotypeQuality
all individuals: 1084
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1620
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6323
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variant carriers: 0

GenotypeQuality
all individuals: 8244
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variant carriers: 0

GenotypeQuality
all individuals: 2070
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13625
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variant carriers: 0

GenotypeQuality
all individuals: 1440
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 505
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variant carriers: 0

GenotypeQuality
all individuals: 951
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variant carriers: 1

GenotypeQuality
all individuals: 1830
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variant carriers: 0

GenotypeQuality
all individuals: 3840
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6728
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14762
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8308
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5798
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.528730971950905e-5
allele num: 54262
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

DP
type: SiteQuality
SIO_000300: 1.132179e6

VQSLOD
type: SiteQuality
SIO_000300: -2.318e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.97e0

GenotypeQuality
all individuals: 8225
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1426
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1878
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3985
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variant carriers: 0

GenotypeQuality
all individuals: 11055
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variant carriers: 0

GenotypeQuality
all individuals: 452
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variant carriers: 0

GenotypeQuality
all individuals: 2113
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6398
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 502
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variant carriers: 0

GenotypeQuality
all individuals: 940
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3838
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3598
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.932665919369178e-5
allele num: 51742
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6358
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.251877816725087e-4
allele num: 7988
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8744
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14316
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

QD
type: SiteQuality
SIO_000300: 9.42e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.1142e6

VQSLOD
type: SiteQuality
SIO_000300: -2.34e-1

GenotypeQuality
all individuals: 2038
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1066
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1433
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variant carriers: 0

GenotypeQuality
all individuals: 2535
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variant carriers: 0

GenotypeQuality
all individuals: 766
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variant carriers: 0

GenotypeQuality
all individuals: 11410
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3580
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3345
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8193
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3840
bin: 9.75e1
variant carriers: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6366
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51762
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.420752565564424e-4
allele num: 8770
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7984
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.968641114982578e-5
allele num: 14350
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

DP
type: SiteQuality
SIO_000300: 1.113695e6

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.67e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.224e0

QD
type: SiteQuality
SIO_000300: 1.149e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-3

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3591
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 370
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5203
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
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variant carriers: 0

GenotypeQuality
all individuals: 6730
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4654
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variant carriers: 0

GenotypeQuality
all individuals: 12213
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2378
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9714
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.014681498899641e-5
allele num: 66342
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e-1

DP
type: SiteQuality
SIO_000300: 2.017627e6

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.45e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

QD
type: SiteQuality
SIO_000300: 1.456e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

GenotypeQuality
all individuals: 3579
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6711
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5147
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16211
bin: 9.75e1
variant carriers: 24

GenotypeQuality
all individuals: 12648
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4617
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2377
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9714
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.04295403165034e-5
allele num: 66350
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.689607229753215e-5
allele num: 11508
num of homozygotes: 0

South Asian
type: Population
allele count: 17
allele frequency: 1.030927835051546e-3
allele num: 16490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.36e-1

QD
type: SiteQuality
SIO_000300: 1.331e1

DP
type: SiteQuality
SIO_000300: 2.020877e6

VQSLOD
type: SiteQuality
SIO_000300: 4.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.211e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5162
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4628
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.013500482160077e-5
allele num: 66368
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9716
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e-1

QD
type: SiteQuality
SIO_000300: 1.224e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.026307e6

GenotypeQuality
all individuals: 534
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3603
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2377
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9716
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506432466632521e-5
allele num: 66382
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.035433e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.91e0

VQSLOD
type: SiteQuality
SIO_000300: 6.04e-1

QD
type: SiteQuality
SIO_000300: 1.357e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 24

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
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variant carriers: 0

GenotypeQuality
all individuals: 16234
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9724
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513775355737209e-4
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 23
allele frequency: 3.460728257598556e-4
allele num: 66460
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
type: SiteQuality
SIO_000300: 4.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.565e0

DP
type: SiteQuality
SIO_000300: 2.047773e6

QD
type: SiteQuality
SIO_000300: 1.223e1

GenotypeQuality
all individuals: 3598
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 9.25e1
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
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66526
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.008e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.945e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.64e-1

QD
type: SiteQuality
SIO_000300: 1.191e1

DP
type: SiteQuality
SIO_000300: 2.052405e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

FS
type: SiteQuality
SIO_000300: 3.648e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.11e-1

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 4684
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5206
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variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3598
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
all individuals: 3611
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66526
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.053268765133172e-4
allele num: 6608
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.64e-1

QD
type: SiteQuality
SIO_000300: 1.191e1

MQRankSum
type: SiteQuality
SIO_000300: -1.008e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.11e-1

FS
type: SiteQuality
SIO_000300: 3.648e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

DP
type: SiteQuality
SIO_000300: 2.052405e6

VQSLOD
type: SiteQuality
SIO_000300: 5.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.945e0

GenotypeQuality
all individuals: 97
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3608
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16931
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66544
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.948e1

QD
type: SiteQuality
SIO_000300: 1.715e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.041e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.719e-1

DP
type: SiteQuality
SIO_000300: 2.054259e6

FS
type: SiteQuality
SIO_000300: 4.135e0

MQRankSum
type: SiteQuality
SIO_000300: -3.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.9e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
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GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 8
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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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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2387
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.055085e6

MQRankSum
type: SiteQuality
SIO_000300: -5.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.043e0

VQSLOD
type: SiteQuality
SIO_000300: 3.85e-1

FS
type: SiteQuality
SIO_000300: 1.083e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

QD
type: SiteQuality
SIO_000300: 1.042e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.43e-1

GenotypeQuality
all individuals: 105
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 43
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GenotypeQuality
all individuals: 16184
bin: 9.75e1
variant carriers: 1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
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: 8618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502358703163967e-5
allele num: 66562
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQ
type: SiteQuality
SIO_000300: 5.745e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-1

FS
type: SiteQuality
SIO_000300: 8.448e0

DP
type: SiteQuality
SIO_000300: 2.055448e6

VQSLOD
type: SiteQuality
SIO_000300: 9.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.14e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.064e0

QD
type: SiteQuality
SIO_000300: 1.335e1

GenotypeQuality
all individuals: 4693
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 7120
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 40
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variant carriers: 0

GenotypeQuality
all individuals: 154
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GenotypeQuality
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GenotypeQuality
all individuals: 16186
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5218
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3610
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21197430614471e-4
allele num: 16502
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9748
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66578
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: -7.07e-1

FS
type: SiteQuality
SIO_000300: 6.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.892e0

VQSLOD
type: SiteQuality
SIO_000300: 5.83e-1

QD
type: SiteQuality
SIO_000300: 1.072e1

DP
type: SiteQuality
SIO_000300: 2.056506e6

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

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3619
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16183
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 92
bin: 2.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.85e-1

FS
type: SiteQuality
SIO_000300: 7.99e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.09e-1

QD
type: SiteQuality
SIO_000300: 1.374e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

DP
type: SiteQuality
SIO_000300: 2.059591e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-2

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4697
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variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
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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GenotypeQuality
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bin: 6.25e1
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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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variant carriers: 0

GenotypeQuality
all individuals: 5218
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.096e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

QD
type: SiteQuality
SIO_000300: 7.94e0

MQRankSum
type: SiteQuality
SIO_000300: -4.52e-1

FS
type: SiteQuality
SIO_000300: 1.019e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
type: SiteQuality
SIO_000300: 2.059643e6

MQ
type: SiteQuality
SIO_000300: 5.841e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.83e-1

GenotypeQuality
all individuals: 10
bin: 3.75e1
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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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
all individuals: 5220
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
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: 9774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66658
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.709e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.143e0

DP
type: SiteQuality
SIO_000300: 2.059689e6

QD
type: SiteQuality
SIO_000300: 1.447e1

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.926e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: -4.956e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.26e0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

East Asian
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: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.992e0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.6e-2

FS
type: SiteQuality
SIO_000300: 4.835e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.059882e6

QD
type: SiteQuality
SIO_000300: 1.679e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.03e-1

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4698
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variant carriers: 0

GenotypeQuality
all individuals: 2388
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500015000150001e-5
allele num: 66666
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

MQRankSum
type: SiteQuality
SIO_000300: -1.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.29e-1

FS
type: SiteQuality
SIO_000300: 1.206e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 2.059933e6

MQ
type: SiteQuality
SIO_000300: 5.979e1

QD
type: SiteQuality
SIO_000300: 1.174e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16185
bin: 9.75e1
variant carriers: 3

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.500045000450004e-5
allele num: 66666
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9774
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 7.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.505e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.21e-1

QD
type: SiteQuality
SIO_000300: 1.174e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 4.082e0

DP
type: SiteQuality
SIO_000300: 2.060113e6

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 19
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9774
num of homozygotes: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.479471120389701e-4
allele num: 8622
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.54e-1

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.545e0

VQSLOD
type: SiteQuality
SIO_000300: 8.68e-1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.19e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.060013e6

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9774
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.16e-1

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.968e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.202e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3614
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2388
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9776
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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European (Finnish)
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Other
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VQSLOD
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FS
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InbreedingCoeff
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MQRankSum
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MQ
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ReadPosRankSum
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QD
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BaseQRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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variant carriers: 1

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

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

Latino
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allele frequency: 0.0e0
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European (Finnish)
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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

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: 1.499970000599988e-5
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VQSLOD
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MQ
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DP
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MQRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
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allele frequency: 0.0e0
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Latino
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East Asian
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allele frequency: 0.0e0
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African
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European (Non-Finnish)
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allele num: 66662
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Other
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QD
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FS
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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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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bin: 9.75e1
variant carriers: 2

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

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

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

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 frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 0

Other
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num of homozygotes: 0

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

African
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East Asian
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European (Non-Finnish)
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Other
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Latino
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European (Finnish)
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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MQ
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FS
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QD
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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South Asian
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num of homozygotes: 0

Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.5001500150015e-5
allele num: 66660
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African
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European (Finnish)
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Latino
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East Asian
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VQSLOD
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MQ
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FS
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele num: 66662
num of homozygotes: 0

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

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17066
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 2.047921359819783e-4
allele num: 9766
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 5.22e-1

QD
type: SiteQuality
SIO_000300: 1.203e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.978e0

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-1

DP
type: SiteQuality
SIO_000300: 2.057895e6

GenotypeQuality
all individuals: 5209
bin: 7.75e1
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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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500780405811022e-5
allele num: 66632
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.82e-1

DP
type: SiteQuality
SIO_000300: 2.0577e6

VQSLOD
type: SiteQuality
SIO_000300: 6.96e-1

QD
type: SiteQuality
SIO_000300: 1.167e1

MQ
type: SiteQuality
SIO_000300: 5.937e1

FS
type: SiteQuality
SIO_000300: 5.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.5e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

FS
type: SiteQuality
SIO_000300: 7.38e-1

QD
type: SiteQuality
SIO_000300: 9.609999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.89e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.21e-1

DP
type: SiteQuality
SIO_000300: 2.057384e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.989e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 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: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.89e-1

FS
type: SiteQuality
SIO_000300: 7.38e-1

QD
type: SiteQuality
SIO_000300: 9.609999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: -5.21e-1

DP
type: SiteQuality
SIO_000300: 2.057384e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.989e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 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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variant carriers: 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: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.989e0

VQSLOD
type: SiteQuality
SIO_000300: 3.89e-1

FS
type: SiteQuality
SIO_000300: 7.38e-1

QD
type: SiteQuality
SIO_000300: 9.609999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

DP
type: SiteQuality
SIO_000300: 2.057384e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160631383472609e-4
allele num: 8616
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.0566e6

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -6.472e-1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 7.86e0

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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bin: 8.25e1
variant carriers: 0

East Asian
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allele count: 1
allele frequency: 1.163061177017911e-4
allele num: 8598
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66564
num of homozygotes: 0

South Asian
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allele count: 0
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

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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variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.515632515632516e-5
allele num: 66528
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 894
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.006253006253006e-5
allele num: 66528
num of homozygotes: 0

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

InbreedingCoeff
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DP
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ReadPosRankSum
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VQSLOD
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MQRankSum
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MQ
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BaseQRankSum
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FS
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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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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3547
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3611
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4680
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503307276007216e-5
allele num: 66520
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-2

FS
type: SiteQuality
SIO_000300: 2.688e0

MQRankSum
type: SiteQuality
SIO_000300: -1.221e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.01e0

DP
type: SiteQuality
SIO_000300: 2.034761e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.299e0

VQSLOD
type: SiteQuality
SIO_000300: 3.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

GenotypeQuality
all individuals: 3600
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16166
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5113
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3457
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 5.75e1
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GenotypeQuality
all individuals: 1086
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13192
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 871
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4665
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504211793020457e-5
allele num: 66480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.026588e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.06e-1

QD
type: SiteQuality
SIO_000300: 1.341e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
all individuals: 16251
bin: 9.75e1
variant carriers: 147

GenotypeQuality
all individuals: 955
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1134
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5096
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4650
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3437
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11471
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 10
allele frequency: 1.51285930408472e-3
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 28
allele frequency: 1.698204754973314e-3
allele num: 16488
num of homozygotes: 1

African
type: Population
allele count: 2
allele frequency: 2.052545155993432e-4
allele num: 9744
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.061655697956356e-4
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 103
allele frequency: 1.549851033735592e-3
allele num: 66458
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.477e1

DP
type: SiteQuality
SIO_000300: 2.01788e6

VQSLOD
type: SiteQuality
SIO_000300: 5.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

GenotypeQuality
all individuals: 7885
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
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variant carriers: 0

GenotypeQuality
all individuals: 247
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variant carriers: 0

GenotypeQuality
all individuals: 423
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variant carriers: 1

GenotypeQuality
all individuals: 577
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variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 928
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.775549188156638e-4
allele num: 2094
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7946
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.55e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.866e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

VQSLOD
type: SiteQuality
SIO_000300: -2.088e0

FS
type: SiteQuality
SIO_000300: 3.01e0

DP
type: SiteQuality
SIO_000300: 5.13471e5

MQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

QD
type: SiteQuality
SIO_000300: 1.203e1

GenotypeQuality
all individuals: 9955
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4389
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25553
bin: 7.5e0
variant carriers: 1

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

GenotypeQuality
all individuals: 551
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variant carriers: 1

GenotypeQuality
all individuals: 506
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variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3114
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 202
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1744
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2094
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9144
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 928
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.257545271629779e-4
allele num: 7952
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.09e-1

DP
type: SiteQuality
SIO_000300: 5.19929e5

VQSLOD
type: SiteQuality
SIO_000300: 4.46e-1

QD
type: SiteQuality
SIO_000300: 1.323e1

FS
type: SiteQuality
SIO_000300: 3.43e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.29e-2

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 411
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3203
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4248
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1156
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2680
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10503
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1744
bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9138
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7942
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2090
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 928
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.35e-2

QD
type: SiteQuality
SIO_000300: 3.364e1

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

DP
type: SiteQuality
SIO_000300: 5.21695e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.342e0

GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2472
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10700
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1744
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 241
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variant carriers: 0

GenotypeQuality
all individuals: 1185
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 198
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2090
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7966
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 914
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.095770326539557e-4
allele num: 9126
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.88e-1

FS
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 5.23466e5

QD
type: SiteQuality
SIO_000300: 1.531e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.29e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e0

VQSLOD
type: SiteQuality
SIO_000300: -1.629e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.62e-1