10-33538344-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538344
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538344
    reference: chr 10
allele count: 3
allele frequency: 4.535833081342607e-5
allele num: 66140
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4612C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.*5C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4612C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4612C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4612C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4612C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4612C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4612C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4612C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4612C>T
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15023
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 941
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2816
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

10-33538347-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538347
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538347
    reference: chr 10
allele count: 4
allele frequency: 6.000780101413184e-5
allele num: 66658
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4609C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4609C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.*2C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4609C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4609C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4609C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4609C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4609C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4609C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4609C>T
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10977
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14717
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21714
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum

10-33538347-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538347
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538347
    reference: chr 10
allele count: 10
allele frequency: 1.500195025353296e-4
allele num: 66658
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4609C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4609C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.*2C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4609C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4609C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4609C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4609C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4609C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4609C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4609C>G
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14717
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21714
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2778
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD

10-33538348-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538348
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538348
    reference: chr 10
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4608C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4608C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4608C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4608C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4608C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4608C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.*1C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4608C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4608C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4608C>A
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14639
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21663
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4669
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5429
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

10-33538352-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538352
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538352
    reference: chr 10
allele count: 107
allele frequency: 1.588385487797637e-3
allele num: 67364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.508G>A
  hgvsp: ENST00000455749.1:c.508G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4604G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4604G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4604G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4604G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4604G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4604G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4604G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4604G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4604G>A
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 1.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11572
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21469
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 14192
  bin: 1.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 3.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 4556
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23275
  bin: 2.25e1
  variant carriers: 1
hgvs: p.Thr170Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

10-33538353-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538353
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538353
    reference: chr 10
allele count: 4
allele frequency: 5.921890267373346e-5
allele num: 67546
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4603C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.507C>T
  hgvsp: ENSP00000390567.1:p.Thr170Met
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4603C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4603C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4603C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4603C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4603C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4603C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4603C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4603C>T
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14051
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3768
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21445
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12479
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr170Met
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP

10-33538368-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538368
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538368
    reference: chr 10
allele count: 2
allele frequency: 2.874719714827804e-5
allele num: 69572
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4588A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4588A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4588A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4588A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.492A>G
  hgvsp: ENSP00000390567.1:p.Tyr165Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4588A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4588A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4588A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4588A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4588A>G
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4162
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13002
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20948
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1921
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4828
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Tyr165Cys
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

10-33538380-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538380
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538380
    reference: chr 10
allele count: 3
allele frequency: 4.164121925489978e-5
allele num: 72044
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4576G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4576G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4576G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4576G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4576G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4576G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4576G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4576G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.480G>A
  hgvsp: ENSP00000390567.1:p.Ser161Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4576G>A
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15065
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11912
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20095
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1527
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1202
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Ser161Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/10-33538383-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538383
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538383
    reference: chr 10
allele count: 1
allele frequency: 1.374910630808997e-5
allele num: 72732
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4573T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4573T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4573T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4573T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.477T>G
  hgvsp: ENSP00000390567.1:p.Leu160Arg
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4573T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4573T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4573T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4573T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4573T>G
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19876
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4132
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1152
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16004
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu160Arg
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

10-33538390-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538390
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538390
    reference: chr 10
allele count: 2
allele frequency: 2.6732249786142e-5
allele num: 74816
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4566T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4566T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4566T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4566T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4566T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4566T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4566T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4566T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.470T>C
  hgvsp: ENST00000455749.1:c.470T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4566T>C
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10502
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3635
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu158Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

10-33538400-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538400
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538400
    reference: chr 10
allele count: 1
allele frequency: 1.278837792214436e-5
allele num: 78196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4556A>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4556A>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4556A>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4556A>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4556A>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.460A>T
  hgvsp: ENST00000455749.1:c.460A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4556A>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4556A>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4556A>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4556A>T
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17715
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8732
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 858
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2793
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 889
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro154Pro
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

10-33538406-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538406
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538406
    reference: chr 10
allele count: 6
allele frequency: 7.477380922708806e-5
allele num: 80242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4550C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4550C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4550C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4550C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.454C>T
  hgvsp: ENST00000455749.1:c.454C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4550C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4550C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4550C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4550C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4550C>T
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7951
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16731
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23082
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro152Pro
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

10-33538407-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538407
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538407
    reference: chr 10
allele count: 1
allele frequency: 1.239157372986369e-5
allele num: 80700
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4549C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4549C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4549C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4549C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4549C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.453C>G
  hgvsp: ENSP00000390567.1:p.Pro152Arg
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4549C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4549C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4549C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4549C>G
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19339
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro152Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

10-33538418-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538418
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538418
    reference: chr 10
allele count: 2
allele frequency: 2.395898222243519e-5
allele num: 83476
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4538A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4538A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4538A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4538A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4538A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4538A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4538A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.442A>G
  hgvsp: ENST00000455749.1:c.442A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4538A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4538A>G
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6814
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1148
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr148Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

10-33538425-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538425
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538425
    reference: chr 10
allele count: 22
allele frequency: 2.585436938842664e-4
allele num: 85092
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4531C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4531C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4531C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4531C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4531C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4531C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4531C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.435C>A
  hgvsp: ENSP00000390567.1:p.Ser146Ter
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4531C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4531C>A
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26494
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5545
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 663
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser146Ter
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

10-33538426-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538426
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538426
    reference: chr 10
allele count: 22
allele frequency: 2.571956323505343e-4
allele num: 85538
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4530T>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4530T>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4530T>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4530T>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4530T>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4530T>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4530T>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.434T>A
  hgvsp: ENSP00000390567.1:p.Ser146Thr
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4530T>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4530T>A
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26938
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5549
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14360
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6233
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1679
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser146Thr
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

10-33538427-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538427
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538427
    reference: chr 10
allele count: 1
allele frequency: 1.164578189779662e-5
allele num: 85868
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4529T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4529T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4529T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4529T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.433T>C
  hgvsp: ENST00000455749.1:c.433T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4529T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4529T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4529T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4529T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4529T>C
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser145Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

10-33538431-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538431
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538431
    reference: chr 10
allele count: 1
allele frequency: 1.15492111888758e-5
allele num: 86586
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4525C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4525C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4525C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4525C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4525C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4525C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4525C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4525C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4525C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.429C>G
  hgvsp: ENSP00000390567.1:p.Ser144Cys
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13849
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5935
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29520
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser144Cys
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/10-33538443-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538443
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538443
    reference: chr 10
allele count: 7
allele frequency: 8.034709946970914e-5
allele num: 87122
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4513G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4513G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4513G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4513G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4513G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4513G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4513G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.417G>T
  hgvsp: ENSP00000390567.1:p.Arg140Leu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4513G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4513G>T
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13493
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27731
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6143
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 7.25e1
  variant carriers: 1
hgvs: p.Arg140Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

10-33538443-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538443
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538443
    reference: chr 10
allele count: 4
allele frequency: 4.591262826840523e-5
allele num: 87122
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.417G>A
  hgvsp: ENSP00000390567.1:p.Arg140Gln
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4513G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4513G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4513G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4513G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4513G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4513G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4513G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4513G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4513G>A
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27731
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13493
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg140Gln
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum

10-33538444-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538444
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538444
    reference: chr 10
allele count: 2
allele frequency: 2.296738631143776e-5
allele num: 87080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4512C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4512C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.416C>T
  hgvsp: ENSP00000390567.1:p.Arg140Ter
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4512C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4512C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4512C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4512C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4512C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4512C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4512C>T
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27644
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29922
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1249
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg140Ter
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

10-33538458-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538458
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538458
    reference: chr 10
allele count: 2
allele frequency: 2.341043168836033e-5
allele num: 85432
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.402G>A
  hgvsp: ENSP00000390567.1:p.Arg135His
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4498G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4498G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4498G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4498G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4498G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4498G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4498G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4498G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4498G>A
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8049
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27629
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1374
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg135His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

10-33538459-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538459
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538459
    reference: chr 10
allele count: 10
allele frequency: 1.172085609132891e-4
allele num: 85318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4497C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.401C>T
  hgvsp: ENSP00000390567.1:p.Arg135Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4497C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4497C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4497C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4497C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4497C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4497C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4497C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4497C>T
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24720
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6150
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1623
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg135Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

10-33538473-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538473
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538473
    reference: chr 10
allele count: 2
allele frequency: 2.456157587070786e-5
allele num: 81428
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4483C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.387C>T
  hgvsp: ENSP00000390567.1:p.Ala130Val
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4483C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4483C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4483C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4483C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4483C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4483C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4483C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4483C>T
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15826
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5523
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22350
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala130Val
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/10-33538477-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538477
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538477
    reference: chr 10
allele count: 7
allele frequency: 8.73406033987972e-5
allele num: 80146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4479G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.383G>T
  hgvsp: ENSP00000390567.1:p.Asp129Tyr
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4479G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4479G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4479G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4479G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4479G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4479G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4479G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4479G>T
  variant of: http://identifiers.org/hgnc/8004
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13614
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17598
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp129Tyr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP

10-33538491-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538491
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538491
    reference: chr 10
allele count: 5
allele frequency: 6.651412760070239e-5
allele num: 75172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4465G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4465G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4465G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4465G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4465G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.383-14G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4465G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4465G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4465G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4465G>A
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10084
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17446
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19474
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4267
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12712
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1188
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29359
  bin: 2.25e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

10-33538495-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538495
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538495
    reference: chr 10
allele count: 2
allele frequency: 2.739650968466617e-5
allele num: 73002
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4461T>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4461T>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4461T>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4461T>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4461T>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4461T>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.383-18T>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4461T>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4461T>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4461T>A
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17715
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7488
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9580
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3532
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

10-33538501-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538501
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538500
    reference: chr 10
allele count: 4
allele frequency: 5.710533078262856e-5
allele num: 70046
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4454delC
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4454delC
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.383-25delC
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4454delC
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4454delC
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4454delC
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4454delC
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4454delC
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4454delC
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4454delC
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21901
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3903
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4655
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1434
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: AG
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/10-33538512-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33538512
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33538512
    reference: chr 10
allele count: 1
allele frequency: 1.579828746563873e-5
allele num: 63298
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+4444T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+4444T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+4444T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+4444T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+4444T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.383-35T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+4444T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+4444T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+4444T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+4444T>G
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20391
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19705
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5384
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7060
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4853
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

10-33542905-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33542905
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33542905
    reference: chr 10
allele count: 3
allele frequency: 2.668184567220463e-5
allele num: 112436
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+51T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+51T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+51T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+51T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+51T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+51T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+51T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+51T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+51T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.382+51T>C
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13554
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7001
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1654
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1265
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-33542915-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33542915
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33542915
    reference: chr 10
allele count: 1
allele frequency: 8.881310170876408e-6
allele num: 112596
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+41T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+41T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+41T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+41T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+41T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+41T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+41T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+41T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+41T>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.382+41T>G
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13630
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1632
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

10-33542917-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33542917
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33542917
    reference: chr 10
allele count: 1
allele frequency: 8.874846908890822e-6
allele num: 112678
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+39A>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+39A>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+39A>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+39A>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+39A>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+39A>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+39A>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.382+39A>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+39A>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+39A>C
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15989
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7011
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3130
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8535
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

10-33542920-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33542920
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33542920
    reference: chr 10
allele count: 1
allele frequency: 8.870595749210517e-6
allele num: 112732
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+36A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+36A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.382+36A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+36A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+36A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+36A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+36A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+36A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+36A>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+36A>G
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13680
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22249
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

10-33542924-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33542924
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33542924
    reference: chr 10
allele count: 11
allele frequency: 9.745034461985507e-5
allele num: 112878
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+32T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+32T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+32T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+32T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+32T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+32T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.382+32T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+32T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+32T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+32T>C
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4583
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-33542926-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33542926
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33542926
    reference: chr 10
allele count: 2
allele frequency: 1.77166749344483e-5
allele num: 112888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+30G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+30G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+30G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+30G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+30G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+30G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+30G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+30G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.382+30G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+30G>A
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3553
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

10-33542929-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33542929
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33542929
    reference: chr 10
allele count: 1
allele frequency: 8.832829862031198e-6
allele num: 113214
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+27T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.382+27T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+27T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+27T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+27T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+27T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+27T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+27T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+27T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+27T>C
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16306
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4587
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3402
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-33542930-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33542930
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33542930
    reference: chr 10
allele count: 3
allele frequency: 2.648538889379359e-5
allele num: 113270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.382+26C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+26C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+26C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+26C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+26C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+26C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+26C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+26C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+26C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+26C>T
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22969
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3142
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

10-33542935-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33542935
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33542935
    reference: chr 10
allele count: 2
allele frequency: 1.760873393203029e-5
allele num: 113580
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.438+21C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.981+21C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.981+21C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.981+21C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.981+21C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.981+21C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.382+21C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.981+21C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.981+21C>G
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.981+21C>G
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

10-33542965-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33542965
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33542965
    reference: chr 10
allele count: 1
allele frequency: 8.473427331887202e-6
allele num: 118016
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.972G>C
  hgvsp: ENSP00000363949.3:p.Glu324Asp
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.972G>C
  hgvsp: ENSP00000265371.3:p.Glu324Asp
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.373G>C
  hgvsp: ENSP00000390567.1:p.Glu125Asp
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.972G>C
  hgvsp: ENSP00000363955.4:p.Glu324Asp
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.972G>C
  hgvsp: ENSP00000363954.5:p.Glu324Asp
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.972G>C
  hgvsp: ENSP00000364001.2:p.Glu324Asp
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.972G>C
  hgvsp: ENSP00000363956.5:p.Glu324Asp
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.972G>C
  hgvsp: ENSP00000408911.2:p.Glu324Asp
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.429G>C
  hgvsp: ENSP00000364009.1:p.Glu143Asp
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.972G>C
  hgvsp: ENSP00000379317.1:p.Glu324Asp
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7025
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu324Asp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

10-33542985-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33542985
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33542985
    reference: chr 10
allele count: 2
allele frequency: 1.662040653514385e-5
allele num: 120334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.952G>A
  hgvsp: ENSP00000379317.1:p.Gly318Arg
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.353G>A
  hgvsp: ENSP00000390567.1:p.Gly119Arg
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.952G>A
  hgvsp: ENSP00000364001.2:p.Gly318Arg
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.409G>A
  hgvsp: ENSP00000364009.1:p.Gly137Arg
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.952G>A
  hgvsp: ENSP00000265371.3:p.Gly318Arg
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.952G>A
  hgvsp: ENSP00000363955.4:p.Gly318Arg
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.952G>A
  hgvsp: ENSP00000363954.5:p.Gly318Arg
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.952G>A
  hgvsp: ENSP00000408911.2:p.Gly318Arg
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.952G>A
  hgvsp: ENSP00000363949.3:p.Gly318Arg
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.952G>A
  hgvsp: ENSP00000363956.5:p.Gly318Arg
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly318Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

10-33542986-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33542986
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33542986
    reference: chr 10
allele count: 4
allele frequency: 3.319998008001195e-5
allele num: 120482
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.951C>T
  hgvsp: ENST00000374821.5:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.951C>T
  hgvsp: ENST00000374823.5:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.951C>T
  hgvsp: ENST00000265371.4:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.951C>T
  hgvsp: ENST00000374867.2:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.951C>T
  hgvsp: ENST00000374816.3:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.352C>T
  hgvsp: ENST00000455749.1:c.352C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.951C>T
  hgvsp: ENST00000432372.2:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.408C>T
  hgvsp: ENST00000374875.1:c.408C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.951C>T
  hgvsp: ENST00000374822.4:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.951C>T
  hgvsp: ENST00000395995.1:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13941
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27430
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro317Pro
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

10-33543002-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543002
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543002
    reference: chr 10
allele count: 1
allele frequency: 8.254230293025175e-6
allele num: 121150
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.935A>G
  hgvsp: ENSP00000364001.2:p.Glu312Gly
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.935A>G
  hgvsp: ENSP00000363956.5:p.Glu312Gly
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.935A>G
  hgvsp: ENSP00000408911.2:p.Glu312Gly
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.935A>G
  hgvsp: ENSP00000363949.3:p.Glu312Gly
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.336A>G
  hgvsp: ENSP00000390567.1:p.Glu113Gly
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.935A>G
  hgvsp: ENSP00000379317.1:p.Glu312Gly
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.935A>G
  hgvsp: ENSP00000363955.4:p.Glu312Gly
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.392A>G
  hgvsp: ENSP00000364009.1:p.Glu131Gly
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.935A>G
  hgvsp: ENSP00000363954.5:p.Glu312Gly
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.935A>G
  hgvsp: ENSP00000265371.3:p.Glu312Gly
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7037
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu312Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP

10-33543004-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543004
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543004
    reference: chr 10
allele count: 1
allele frequency: 8.251778258214646e-6
allele num: 121186
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.933T>C
  hgvsp: ENST00000265371.4:c.933T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.933T>C
  hgvsp: ENST00000395995.1:c.933T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.933T>C
  hgvsp: ENST00000374867.2:c.933T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.933T>C
  hgvsp: ENST00000374823.5:c.933T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.334T>C
  hgvsp: ENST00000455749.1:c.334T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.390T>C
  hgvsp: ENST00000374875.1:c.390T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.933T>C
  hgvsp: ENST00000432372.2:c.933T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.933T>C
  hgvsp: ENST00000374816.3:c.933T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.933T>C
  hgvsp: ENST00000374822.4:c.933T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.933T>C
  hgvsp: ENST00000374821.5:c.933T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4640
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro311Pro
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

10-33543006-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543006
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543006
    reference: chr 10
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.931C>T
  hgvsp: ENSP00000363954.5:p.Pro311Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.388C>T
  hgvsp: ENSP00000364009.1:p.Pro130Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.332C>T
  hgvsp: ENSP00000390567.1:p.Pro112Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.931C>T
  hgvsp: ENSP00000363949.3:p.Pro311Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.931C>T
  hgvsp: ENSP00000408911.2:p.Pro311Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.931C>T
  hgvsp: ENSP00000363956.5:p.Pro311Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.931C>T
  hgvsp: ENSP00000265371.3:p.Pro311Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.931C>T
  hgvsp: ENSP00000364001.2:p.Pro311Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.931C>T
  hgvsp: ENSP00000379317.1:p.Pro311Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.931C>T
  hgvsp: ENSP00000363955.4:p.Pro311Ser
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17767
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro311Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/10-33543017-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543017
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543017
    reference: chr 10
allele count: 5
allele frequency: 4.123439278233189e-5
allele num: 121258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.377G>T
  hgvsp: ENSP00000364009.1:p.Arg126Leu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.920G>T
  hgvsp: ENSP00000363949.3:p.Arg307Leu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.920G>T
  hgvsp: ENSP00000363955.4:p.Arg307Leu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.920G>T
  hgvsp: ENSP00000364001.2:p.Arg307Leu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.920G>T
  hgvsp: ENSP00000363954.5:p.Arg307Leu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.920G>T
  hgvsp: ENSP00000363956.5:p.Arg307Leu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.920G>T
  hgvsp: ENSP00000379317.1:p.Arg307Leu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.321G>T
  hgvsp: ENSP00000390567.1:p.Arg108Leu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.920G>T
  hgvsp: ENSP00000265371.3:p.Arg307Leu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.920G>T
  hgvsp: ENSP00000408911.2:p.Arg307Leu
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4637
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg307Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

10-33543018-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543018
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543018
    reference: chr 10
allele count: 2
allele frequency: 1.649457328538911e-5
allele num: 121252
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.919C>T
  hgvsp: ENSP00000265371.3:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.919C>T
  hgvsp: ENSP00000363949.3:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.919C>T
  hgvsp: ENSP00000363954.5:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.320C>T
  hgvsp: ENSP00000390567.1:p.Arg108Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.919C>T
  hgvsp: ENSP00000408911.2:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.919C>T
  hgvsp: ENSP00000379317.1:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.919C>T
  hgvsp: ENSP00000363955.4:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.919C>T
  hgvsp: ENSP00000364001.2:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.919C>T
  hgvsp: ENSP00000363956.5:p.Arg307Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.376C>T
  hgvsp: ENSP00000364009.1:p.Arg126Cys
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13950
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg307Cys
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

10-33543024-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543024
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543024
    reference: chr 10
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.913C>T
  hgvsp: ENSP00000363955.4:p.Arg305Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.913C>T
  hgvsp: ENSP00000408911.2:p.Arg305Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.370C>T
  hgvsp: ENSP00000364009.1:p.Arg124Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.913C>T
  hgvsp: ENSP00000363956.5:p.Arg305Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.913C>T
  hgvsp: ENSP00000379317.1:p.Arg305Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.913C>T
  hgvsp: ENSP00000364001.2:p.Arg305Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.913C>T
  hgvsp: ENSP00000363954.5:p.Arg305Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.314C>T
  hgvsp: ENSP00000390567.1:p.Arg106Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.913C>T
  hgvsp: ENSP00000363949.3:p.Arg305Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.913C>T
  hgvsp: ENSP00000265371.3:p.Arg305Cys
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3560
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg305Cys
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD

10-33543041-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543041
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543041
    reference: chr 10
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.896C>T
  hgvsp: ENSP00000379317.1:p.Thr299Ile
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.896C>T
  hgvsp: ENSP00000408911.2:p.Thr299Ile
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.896C>T
  hgvsp: ENSP00000363955.4:p.Thr299Ile
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.297C>T
  hgvsp: ENSP00000390567.1:p.Thr100Ile
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.353C>T
  hgvsp: ENSP00000364009.1:p.Thr118Ile
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.896C>T
  hgvsp: ENSP00000265371.3:p.Thr299Ile
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.896C>T
  hgvsp: ENSP00000363949.3:p.Thr299Ile
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.896C>T
  hgvsp: ENSP00000364001.2:p.Thr299Ile
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.896C>T
  hgvsp: ENSP00000363954.5:p.Thr299Ile
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.896C>T
  hgvsp: ENSP00000363956.5:p.Thr299Ile
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr299Ile
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

10-33543052-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543052
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543052
    reference: chr 10
allele count: 2
allele frequency: 1.649049323065253e-5
allele num: 121282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.342C>T
  hgvsp: ENST00000374875.1:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.885C>T
  hgvsp: ENST00000374821.5:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.885C>T
  hgvsp: ENST00000374823.5:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.286C>T
  hgvsp: ENST00000455749.1:c.286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.885C>T
  hgvsp: ENST00000374822.4:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.885C>T
  hgvsp: ENST00000374867.2:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.885C>T
  hgvsp: ENST00000395995.1:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.885C>T
  hgvsp: ENST00000432372.2:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.885C>T
  hgvsp: ENST00000374816.3:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.885C>T
  hgvsp: ENST00000265371.4:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser295Ser
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

10-33543053-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543053
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543053
    reference: chr 10
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.884C>G
  hgvsp: ENSP00000363949.3:p.Ser295Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.884C>G
  hgvsp: ENSP00000379317.1:p.Ser295Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.884C>G
  hgvsp: ENSP00000363955.4:p.Ser295Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.285C>G
  hgvsp: ENSP00000390567.1:p.Ser96Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.884C>G
  hgvsp: ENSP00000364001.2:p.Ser295Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.884C>G
  hgvsp: ENSP00000363956.5:p.Ser295Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.884C>G
  hgvsp: ENSP00000265371.3:p.Ser295Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.884C>G
  hgvsp: ENSP00000408911.2:p.Ser295Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.341C>G
  hgvsp: ENSP00000364009.1:p.Ser114Cys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.884C>G
  hgvsp: ENSP00000363954.5:p.Ser295Cys
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13936
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser295Cys
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum

10-33543066-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543066
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543066
    reference: chr 10
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.871A>T
  hgvsp: ENSP00000363949.3:p.Ile291Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.871A>T
  hgvsp: ENSP00000363956.5:p.Ile291Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.328A>T
  hgvsp: ENSP00000364009.1:p.Ile110Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.272A>T
  hgvsp: ENSP00000390567.1:p.Ile92Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.871A>T
  hgvsp: ENSP00000265371.3:p.Ile291Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.871A>T
  hgvsp: ENSP00000364001.2:p.Ile291Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.871A>T
  hgvsp: ENSP00000363955.4:p.Ile291Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.871A>T
  hgvsp: ENSP00000408911.2:p.Ile291Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.871A>T
  hgvsp: ENSP00000363954.5:p.Ile291Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.871A>T
  hgvsp: ENSP00000379317.1:p.Ile291Phe
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8518
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ile291Phe
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-33543070-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543070
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543070
    reference: chr 10
allele count: 1
allele frequency: 8.25218682950982e-6
allele num: 121180
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.867C>A
  hgvsp: ENSP00000408911.2:p.Asp289Glu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.867C>A
  hgvsp: ENSP00000265371.3:p.Asp289Glu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.268C>A
  hgvsp: ENSP00000390567.1:p.Asp90Glu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.867C>A
  hgvsp: ENSP00000364001.2:p.Asp289Glu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.867C>A
  hgvsp: ENSP00000363949.3:p.Asp289Glu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.867C>A
  hgvsp: ENSP00000363955.4:p.Asp289Glu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.324C>A
  hgvsp: ENSP00000364009.1:p.Asp108Glu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.867C>A
  hgvsp: ENSP00000363954.5:p.Asp289Glu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.867C>A
  hgvsp: ENSP00000379317.1:p.Asp289Glu
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.867C>A
  hgvsp: ENSP00000363956.5:p.Asp289Glu
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12133
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3554
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp289Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

10-33543072-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543072
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543072
    reference: chr 10
allele count: 1
allele frequency: 8.253685270473266e-6
allele num: 121158
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.266G>A
  hgvsp: ENSP00000390567.1:p.Asp90Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.865G>A
  hgvsp: ENSP00000364001.2:p.Asp289Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.865G>A
  hgvsp: ENSP00000408911.2:p.Asp289Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.322G>A
  hgvsp: ENSP00000364009.1:p.Asp108Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.865G>A
  hgvsp: ENSP00000363956.5:p.Asp289Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.865G>A
  hgvsp: ENSP00000363955.4:p.Asp289Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.865G>A
  hgvsp: ENSP00000363954.5:p.Asp289Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.865G>A
  hgvsp: ENSP00000363949.3:p.Asp289Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.865G>A
  hgvsp: ENSP00000265371.3:p.Asp289Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.865G>A
  hgvsp: ENSP00000379317.1:p.Asp289Asn
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17784
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8456
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp289Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

10-33543073-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543073
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543073
    reference: chr 10
allele count: 1
allele frequency: 8.253821519363466e-6
allele num: 121156
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.864T>C
  hgvsp: ENST00000265371.4:c.864T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.864T>C
  hgvsp: ENST00000374816.3:c.864T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.864T>C
  hgvsp: ENST00000432372.2:c.864T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.864T>C
  hgvsp: ENST00000374867.2:c.864T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.864T>C
  hgvsp: ENST00000374821.5:c.864T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.864T>C
  hgvsp: ENST00000374822.4:c.864T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.321T>C
  hgvsp: ENST00000374875.1:c.321T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.864T>C
  hgvsp: ENST00000374823.5:c.864T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.864T>C
  hgvsp: ENST00000395995.1:c.864T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.265T>C
  hgvsp: ENST00000455749.1:c.265T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser288Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

10-33543074-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543074
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543074
    reference: chr 10
allele count: 1
allele frequency: 8.253957772752034e-6
allele num: 121154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.863C>T
  hgvsp: ENSP00000408911.2:p.Ser288Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.863C>T
  hgvsp: ENSP00000265371.3:p.Ser288Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.863C>T
  hgvsp: ENSP00000363955.4:p.Ser288Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.863C>T
  hgvsp: ENSP00000363956.5:p.Ser288Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.863C>T
  hgvsp: ENSP00000379317.1:p.Ser288Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.863C>T
  hgvsp: ENSP00000364001.2:p.Ser288Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.264C>T
  hgvsp: ENSP00000390567.1:p.Ser89Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.320C>T
  hgvsp: ENSP00000364009.1:p.Ser107Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.863C>T
  hgvsp: ENSP00000363949.3:p.Ser288Phe
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.863C>T
  hgvsp: ENSP00000363954.5:p.Ser288Phe
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12101
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser288Phe
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

10-33543078-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543078
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543078
    reference: chr 10
allele count: 2
allele frequency: 1.651773178507128e-5
allele num: 121082
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.859C>A
  hgvsp: ENSP00000379317.1:p.His287Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.859C>A
  hgvsp: ENSP00000363956.5:p.His287Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.260C>A
  hgvsp: ENSP00000390567.1:p.His88Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.316C>A
  hgvsp: ENSP00000364009.1:p.His106Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.859C>A
  hgvsp: ENSP00000364001.2:p.His287Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.859C>A
  hgvsp: ENSP00000363949.3:p.His287Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.859C>A
  hgvsp: ENSP00000408911.2:p.His287Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.859C>A
  hgvsp: ENSP00000363954.5:p.His287Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.859C>A
  hgvsp: ENSP00000265371.3:p.His287Asn
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.859C>A
  hgvsp: ENSP00000363955.4:p.His287Asn
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13933
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17784
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7033
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His287Asn
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-33543080-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543080
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543080
    reference: chr 10
allele count: 5
allele frequency: 4.133597883597883e-5
allele num: 120960
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.857T>G
  hgvsp: ENSP00000379317.1:p.Ile286Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.857T>G
  hgvsp: ENSP00000363949.3:p.Ile286Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.857T>G
  hgvsp: ENSP00000408911.2:p.Ile286Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.314T>G
  hgvsp: ENSP00000364009.1:p.Ile105Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.857T>G
  hgvsp: ENSP00000265371.3:p.Ile286Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.857T>G
  hgvsp: ENSP00000363956.5:p.Ile286Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.857T>G
  hgvsp: ENSP00000363955.4:p.Ile286Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.857T>G
  hgvsp: ENSP00000364001.2:p.Ile286Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.258T>G
  hgvsp: ENSP00000390567.1:p.Ile87Ser
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.857T>G
  hgvsp: ENSP00000363954.5:p.Ile286Ser
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13931
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3174
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ile286Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

10-33543084-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543084
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543084
    reference: chr 10
allele count: 1
allele frequency: 8.272256506129742e-6
allele num: 120886
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.310G>A
  hgvsp: ENSP00000364009.1:p.Glu104Lys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.853G>A
  hgvsp: ENSP00000363955.4:p.Glu285Lys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.254G>A
  hgvsp: ENSP00000390567.1:p.Glu86Lys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.853G>A
  hgvsp: ENSP00000265371.3:p.Glu285Lys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.853G>A
  hgvsp: ENSP00000364001.2:p.Glu285Lys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.853G>A
  hgvsp: ENSP00000379317.1:p.Glu285Lys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.853G>A
  hgvsp: ENSP00000363949.3:p.Glu285Lys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.853G>A
  hgvsp: ENSP00000363956.5:p.Glu285Lys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.853G>A
  hgvsp: ENSP00000363954.5:p.Glu285Lys
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.853G>A
  hgvsp: ENSP00000408911.2:p.Glu285Lys
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7036
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu285Lys
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

10-33543088-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543088
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543088
    reference: chr 10
allele count: 1
allele frequency: 8.276501357346223e-6
allele num: 120824
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.849A>G
  hgvsp: ENST00000374867.2:c.849A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.849A>G
  hgvsp: ENST00000374821.5:c.849A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.849A>G
  hgvsp: ENST00000265371.4:c.849A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.849A>G
  hgvsp: ENST00000395995.1:c.849A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.849A>G
  hgvsp: ENST00000374816.3:c.849A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.849A>G
  hgvsp: ENST00000374823.5:c.849A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.250A>G
  hgvsp: ENST00000455749.1:c.250A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.849A>G
  hgvsp: ENST00000432372.2:c.849A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.849A>G
  hgvsp: ENST00000374822.4:c.849A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.306A>G
  hgvsp: ENST00000374875.1:c.306A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13924
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser283Ser
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

10-33543131-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543131
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543131
    reference: chr 10
allele count: 1
allele frequency: 8.43668269636379e-6
allele num: 118530
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.815-9T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.815-9T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.216-9T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.815-9T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.815-9T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.815-9T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.815-9T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.815-9T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.815-9T>C
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.272-9T>C
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13785
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24404
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/10-33543136-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543136
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543136
    reference: chr 10
allele count: 1
allele frequency: 8.475581848693913e-6
allele num: 117986
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.815-14G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.272-14G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.815-14G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.216-14G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.815-14G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.815-14G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.815-14G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.815-14G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.815-14G>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.815-14G>T
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

10-33543139-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543139
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543139
    reference: chr 10
allele count: 2
allele frequency: 1.696122663591031e-5
allele num: 117916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.815-17C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.815-17C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.815-17C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.272-17C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.216-17C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.815-17C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.815-17C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.815-17C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.815-17C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.815-17C>T
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13731
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7011
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4534
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3089
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3627
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

10-33543140-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543140
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543140
    reference: chr 10
allele count: 1
allele frequency: 8.487811502682149e-6
allele num: 117816
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.815-18C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.216-18C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.815-18C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.272-18C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.815-18C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.815-18C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.815-18C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.815-18C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.815-18C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.815-18C>T
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 13710
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

10-33543140-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543140
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543141
    reference: chr 10
allele count: 1
allele frequency: 8.487811502682149e-6
allele num: 117816
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.815-19dupG
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.815-19dupG
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.216-19dupG
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.272-19dupG
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.815-19dupG
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.815-19dupG
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.815-19dupG
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.815-19dupG
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.815-19dupG
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.815-19dupG
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13710
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2363
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3081
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3710
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

10-33543141-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543141
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543141
    reference: chr 10
allele count: 1
allele frequency: 8.506294658046955e-6
allele num: 117560
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.815-19G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.815-19G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.815-19G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.272-19G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.815-19G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.815-19G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.216-19G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.815-19G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.815-19G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.815-19G>A
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3076
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

10-33543143-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543143
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543143
    reference: chr 10
allele count: 2
allele frequency: 1.702533369654045e-5
allele num: 117472
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.815-21G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.815-21G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.815-21G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.272-21G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.815-21G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.815-21G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.216-21G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.815-21G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.815-21G>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.815-21G>A
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6994
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16333
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

10-33543147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543147
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543147
    reference: chr 10
allele count: 1
allele frequency: 8.529948649709128e-6
allele num: 117234
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.815-25C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.815-25C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.815-25C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.815-25C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.815-25C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.815-25C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.815-25C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.815-25C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.272-25C>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.216-25C>T
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6988
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16202
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8499
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

10-33543151-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543151
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543151
    reference: chr 10
allele count: 1
allele frequency: 8.559738414394057e-6
allele num: 116826
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.815-29A>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.815-29A>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.815-29A>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.815-29A>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.815-29A>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.815-29A>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.815-29A>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.216-29A>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.272-29A>T
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.815-29A>T
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3022
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21891
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

10-33543164-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33543164
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 33543164
    reference: chr 10
allele count: 6
allele frequency: 5.243655177235545e-5
allele num: 114424
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000265371
  ensembl transcript: ENST00000265371
  gene symbol: NRP1
  hgvsc: ENST00000265371.4:c.815-42C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363954
  ensembl transcript: ENST00000374821
  gene symbol: NRP1
  hgvsc: ENST00000374821.5:c.815-42C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000379317
  ensembl transcript: ENST00000395995
  gene symbol: NRP1
  hgvsc: ENST00000395995.1:c.815-42C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363949
  ensembl transcript: ENST00000374816
  gene symbol: NRP1
  hgvsc: ENST00000374816.3:c.815-42C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363955
  ensembl transcript: ENST00000374822
  gene symbol: NRP1
  hgvsc: ENST00000374822.4:c.815-42C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000390567
  ensembl transcript: ENST00000455749
  gene symbol: NRP1
  hgvsc: ENST00000455749.1:c.216-42C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364001
  ensembl transcript: ENST00000374867
  gene symbol: NRP1
  hgvsc: ENST00000374867.2:c.815-42C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000364009
  ensembl transcript: ENST00000374875
  gene symbol: NRP1
  hgvsc: ENST00000374875.1:c.272-42C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000363956
  ensembl transcript: ENST00000374823
  gene symbol: NRP1
  hgvsc: ENST00000374823.5:c.815-42C>A
  variant of: http://identifiers.org/hgnc/8004
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099250
  ensembl protein: ENSP00000408911
  ensembl transcript: ENST00000432372
  gene symbol: NRP1
  hgvsc: ENST00000432372.2:c.815-42C>A
  variant of: http://identifiers.org/hgnc/8004
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13053
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6604
  bin: 3.75e1
  variant carriers: 1
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 2508
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1479
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10731
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23269
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4770
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 80
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5597
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 8.593033913840513e-5
allele num: 34912
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4860
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5304
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.771e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

FS
type: SiteQuality
SIO_000300: 1.3016e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 9.34e0

DP
type: SiteQuality
SIO_000300: 7.88237e5

MQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

GenotypeQuality
all individuals: 61
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1024
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2433
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 834
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4694
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2778
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1415
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5474
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11278
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23285
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10680
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 8.514019752525826e-5
allele num: 35236
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.853224610822832e-4
allele num: 5396
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5318
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

QD
type: SiteQuality
SIO_000300: 1.3e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.63e-1

FS
type: SiteQuality
SIO_000300: 3.538e0

DP
type: SiteQuality
SIO_000300: 7.95966e5

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

GenotypeQuality
all individuals: 223
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23285
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 326
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4694
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11278
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5474
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 834
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2433
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 969
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 803
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 2.838006584175275e-4
allele num: 35236
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4910
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10680
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

FS
type: SiteQuality
SIO_000300: 3.538e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

DP
type: SiteQuality
SIO_000300: 7.95966e5

VQSLOD
type: SiteQuality
SIO_000300: 8.63e-1

QD
type: SiteQuality
SIO_000300: 1.3e1

GenotypeQuality
all individuals: 78
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23228
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2745
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 831
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2405
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11428
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10690
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.836396641706376e-5
allele num: 35256
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4910
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.98459e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.05e-2

QD
type: SiteQuality
SIO_000300: 1.008e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.47e-1

GenotypeQuality
all individuals: 5241
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2309
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 886
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1059
bin: 9.75e1
variant carriers: 104

GenotypeQuality
all individuals: 177
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2607
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 12237
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 265
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1042
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 41
bin: 8.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4954
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5384
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 3.644314868804665e-4
allele num: 5488
num of homozygotes: 0

South Asian
type: Population
allele count: 88
allele frequency: 8.148148148148147e-3
allele num: 10800
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.773049645390071e-3
allele num: 564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 4.493624669999438e-4
allele num: 35606
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.18e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

DP
type: SiteQuality
SIO_000300: 8.11211e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.31e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.266e0

GenotypeQuality
all individuals: 38
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4519
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2600
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5193
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1141
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 901
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23332
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 212
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 288
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2260
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 8.25e1
variant carriers: 1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4578
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5510
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.016129032258065e-4
allele num: 4960
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.851851851851852e-4
allele num: 10800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.798611888503302e-5
allele num: 35732
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.501e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.082e1

VQSLOD
type: SiteQuality
SIO_000300: 9.02e-1

DP
type: SiteQuality
SIO_000300: 8.13414e5

GenotypeQuality
all individuals: 85
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 22899
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1110
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1131
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2506
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 816
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.805706031058144e-4
allele num: 5538
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10944
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.705627705627706e-5
allele num: 36960
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5150
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4678
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

DP
type: SiteQuality
SIO_000300: 8.39335e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

FS
type: SiteQuality
SIO_000300: 9.231999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e0

QD
type: SiteQuality
SIO_000300: 7.39e0

GenotypeQuality
all individuals: 83
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 8.989572096368213e-5
allele num: 11124
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4772
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5734
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 3.275466754012447e-4
allele num: 6106
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5314
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.322e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.995e0

VQSLOD
type: SiteQuality
SIO_000300: 4.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

MQ
type: SiteQuality
SIO_000300: 5.899e1

FS
type: SiteQuality
SIO_000300: 8.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.26e-1

DP
type: SiteQuality
SIO_000300: 8.71362e5

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5760
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4824
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.574930476877124e-5
allele num: 38836
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.96e-1

DP
type: SiteQuality
SIO_000300: 8.81514e5

FS
type: SiteQuality
SIO_000300: 6.862e0

VQSLOD
type: SiteQuality
SIO_000300: 6.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

QD
type: SiteQuality
SIO_000300: 1.154e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5508
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.550387596899225e-4
allele num: 6450
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4914
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40132
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.701258931609391e-4
allele num: 5878
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e0

QD
type: SiteQuality
SIO_000300: 1.243e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.505e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.26e0

DP
type: SiteQuality
SIO_000300: 9.11678e5

GenotypeQuality
all individuals: 113
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 554
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variant carriers: 0

GenotypeQuality
all individuals: 443
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 60
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GenotypeQuality
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GenotypeQuality
all individuals: 910
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GenotypeQuality
all individuals: 1443
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variant carriers: 0

GenotypeQuality
all individuals: 1000
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GenotypeQuality
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GenotypeQuality
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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: 100
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GenotypeQuality
all individuals: 43
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6864
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.645278051990786e-4
allele num: 6078
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5762
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5076
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e-1

QD
type: SiteQuality
SIO_000300: 1.119e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

DP
type: SiteQuality
SIO_000300: 9.57283e5

VQSLOD
type: SiteQuality
SIO_000300: 3.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -9.88e-1

FS
type: SiteQuality
SIO_000300: 3.053e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.051e0

GenotypeQuality
all individuals: 601
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7172
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5146
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 1.019367991845056e-3
allele num: 5886
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6172
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11702
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

FS
type: SiteQuality
SIO_000300: 1.839e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.543e1

DP
type: SiteQuality
SIO_000300: 9.85222e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.975e0

VQSLOD
type: SiteQuality
SIO_000300: 3.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11732
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5924
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43788
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.38121546961326e-4
allele num: 7240
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.90015e5

QD
type: SiteQuality
SIO_000300: 1.057e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.843e0

VQSLOD
type: SiteQuality
SIO_000300: 9.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.06e0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45422
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5288
num of homozygotes: 0

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

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

South Asian
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allele count: 2
allele frequency: 1.67897918065816e-4
allele num: 11912
num of homozygotes: 0

FS
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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QD
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 22

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.551831160769708e-4
allele num: 6444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 3.88014658331537e-4
allele num: 46390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12004
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.819709702062643e-4
allele num: 7854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5368
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

QD
type: SiteQuality
SIO_000300: 1.476e1

FS
type: SiteQuality
SIO_000300: 2.485e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.233e0

DP
type: SiteQuality
SIO_000300: 1.044494e6

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 22

GenotypeQuality
all individuals: 300
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.549426712116517e-4
allele num: 6454
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.786922494319616e-4
allele num: 7922
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12040
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 3.856536829926726e-4
allele num: 46674
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6392
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.488e1

FS
type: SiteQuality
SIO_000300: 2.479e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.113e0

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e-1

DP
type: SiteQuality
SIO_000300: 1.048314e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46884
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12066
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.257861635220126e-4
allele num: 7950
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 672
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.3e-2

QD
type: SiteQuality
SIO_000300: 7.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.051763e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.16e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.144e0

MQ
type: SiteQuality
SIO_000300: 5.907e1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8020
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47338
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.536098310291859e-4
allele num: 6510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 676
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12100
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

QD
type: SiteQuality
SIO_000300: 1.202e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

DP
type: SiteQuality
SIO_000300: 1.060603e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.192e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.99e0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5456
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 670
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.526717557251908e-4
allele num: 6550
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 7.438631291842301e-4
allele num: 8066
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47666
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12168
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e-1

DP
type: SiteQuality
SIO_000300: 1.066605e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.476e0

FS
type: SiteQuality
SIO_000300: 1.0424e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.87e-1

QD
type: SiteQuality
SIO_000300: 8.300000000000001e0

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: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 670
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.643655489809336e-4
allele num: 12168
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8066
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.526717557251908e-4
allele num: 6550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.097931439600554e-5
allele num: 47666
num of homozygotes: 0

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 1.0424e1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12166
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.19797657529071e-5
allele num: 47642
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5458
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 674
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8036
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.73e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

VQSLOD
type: SiteQuality
SIO_000300: -7.098e-1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.06731e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 304
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variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.289636238846946e-5
allele num: 46624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6440
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
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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

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
allele num: 6434
num of homozygotes: 0

European (Finnish)
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allele count: 4
allele frequency: 7.432181345224824e-4
allele num: 5382
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.506024096385542e-3
allele num: 664
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 1.074113856068743e-4
allele num: 46550
num of homozygotes: 0

BaseQRankSum
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InbreedingCoeff
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SIO_000300: -3.5e-3

ClippingRankSum
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FS
type: SiteQuality
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MQ
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MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

ReadPosRankSum
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SIO_000300: 6.48e-1

QD
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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African
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allele count: 2
allele frequency: 3.26477309826967e-4
allele num: 6126
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11740
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5218
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 44322
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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DP
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FS
type: SiteQuality
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QD
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

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

South Asian
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allele frequency: 6.019951840385277e-4
allele num: 11628
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.73e-1

InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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FS
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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QD
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MQ
type: SiteQuality
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DP
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SIO_000300: 9.37259e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4960
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5496
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 40760
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6616
num of homozygotes: 0

African
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allele count: 5
allele frequency: 8.84016973125884e-4
allele num: 5656
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.037e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

ReadPosRankSum
type: SiteQuality
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FS
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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DP
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 576
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 5.059960532307848e-5
allele num: 39526
num of homozygotes: 0

VQSLOD
type: SiteQuality
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ClippingRankSum
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FS
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MQ
type: SiteQuality
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QD
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DP
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.055798975874993e-4
allele num: 37886
num of homozygotes: 0

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

East Asian
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African
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Latino
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Other
type: Population
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European (Non-Finnish)
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allele frequency: 3.102795618852586e-5
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South Asian
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VQSLOD
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MQRankSum
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DP
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MQ
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FS
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7988
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64524
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.641342074816814e-5
allele num: 10372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.978e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-2

MQ
type: SiteQuality
SIO_000300: 5.93e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

QD
type: SiteQuality
SIO_000300: 8.41e0

FS
type: SiteQuality
SIO_000300: 2.618e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.676e0

DP
type: SiteQuality
SIO_000300: 1.852901e6

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64546
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10422
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.170411985018727e-4
allele num: 8544
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.88e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

FS
type: SiteQuality
SIO_000300: 3.403e0

DP
type: SiteQuality
SIO_000300: 1.855438e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.92e0

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.03e-1

QD
type: SiteQuality
SIO_000300: 9.460000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.161e0

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64552
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.169864295741694e-4
allele num: 8548
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.41e-1

QD
type: SiteQuality
SIO_000300: 1.352e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

DP
type: SiteQuality
SIO_000300: 1.858597e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 11

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64594
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.222841225626741e-4
allele num: 11488
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.675081813931744e-4
allele num: 8556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.476876421531463e-5
allele num: 10552
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.953e1

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

MQRankSum
type: SiteQuality
SIO_000300: 1.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e0

FS
type: SiteQuality
SIO_000300: 1.435e0

QD
type: SiteQuality
SIO_000300: 1.579e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

DP
type: SiteQuality
SIO_000300: 1.864333e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.45e-1

GenotypeQuality
all individuals: 22743
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8076
bin: 6.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.704735376044568e-5
allele num: 11488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.548275221403357e-5
allele num: 64588
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10568
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.299e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.159999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.172e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.767e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.42e-1

DP
type: SiteQuality
SIO_000300: 1.866539e6

VQSLOD
type: SiteQuality
SIO_000300: 7.74e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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: 0
allele frequency: 0.0e0
allele num: 10766
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545738399233314e-5
allele num: 64694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.09e0

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -1.121e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.952e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.870985e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.62e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

European (Finnish)
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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: 10272
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.636211905792174e-5
allele num: 64708
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.367e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

VQSLOD
type: SiteQuality
SIO_000300: 9.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

FS
type: SiteQuality
SIO_000300: 3.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.45e-1

DP
type: SiteQuality
SIO_000300: 1.871849e6

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.543448062972681e-5
allele num: 64790
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 9.094216078574027e-5
allele num: 10996
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

ClippingRankSum
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.097e1

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

East Asian
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.518971959777622e-5
allele num: 65834
num of homozygotes: 0

QD
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BaseQRankSum
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FS
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ReadPosRankSum
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MQ
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InbreedingCoeff
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SIO_000300: 5.1e-3

MQRankSum
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VQSLOD
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ClippingRankSum
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SIO_000300: -2.96e-1

DP
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SIO_000300: 1.917438e6

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

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

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

East Asian
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allele count: 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: 3.011413256241154e-5
allele num: 66414
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South Asian
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQ
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FS
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BaseQRankSum
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MQRankSum
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QD
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DP
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InbreedingCoeff
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SIO_000300: -2.0e-4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 3.009510051763573e-5
allele num: 66456
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
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East Asian
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allele frequency: 2.315886984715146e-4
allele num: 8636
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VQSLOD
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MQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 6.1020258725897e-5
allele num: 16388
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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FS
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InbreedingCoeff
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SIO_000300: 1.85e-2

QD
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SIO_000300: 1.25e1

MQRankSum
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SIO_000300: 9.13e-1

DP
type: SiteQuality
SIO_000300: 1.95199e6

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50073536032656e-5
allele num: 66634
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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East Asian
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South Asian
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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FS
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ClippingRankSum
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MQRankSum
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QD
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BaseQRankSum
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 4.318535152876144e-4
allele num: 11578
num of homozygotes: 0

East Asian
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European (Non-Finnish)
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African
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Other
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European (Finnish)
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South Asian
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VQSLOD
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FS
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MQ
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DP
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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East Asian
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South Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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DP
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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FS
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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QD
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SIO_000300: 1.559e1

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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: 7.25e1
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: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5001500150015e-5
allele num: 66660
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.49e-2

MQ
type: SiteQuality
SIO_000300: 5.875e1

QD
type: SiteQuality
SIO_000300: 7.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.47e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.74e-1

DP
type: SiteQuality
SIO_000300: 1.95391e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.767e0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2373
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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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: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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: 8646
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.04e0

MQ
type: SiteQuality
SIO_000300: 5.918e1

DP
type: SiteQuality
SIO_000300: 1.9537e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-2

FS
type: SiteQuality
SIO_000300: 5.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.39e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e-1

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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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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: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000300030003e-5
allele num: 66660
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 8.329000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.67e-1

QD
type: SiteQuality
SIO_000300: 1.336e1

MQRankSum
type: SiteQuality
SIO_000300: 5.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.209e0

DP
type: SiteQuality
SIO_000300: 1.952991e6

VQSLOD
type: SiteQuality
SIO_000300: 1.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.82e-1

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: 2.5e0
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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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28035
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.952883e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.11e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

VQSLOD
type: SiteQuality
SIO_000300: -4.414e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.380000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.721e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66630
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

QD
type: SiteQuality
SIO_000300: 1.531e1

FS
type: SiteQuality
SIO_000300: 1.816e0

VQSLOD
type: SiteQuality
SIO_000300: 3.34e-1

DP
type: SiteQuality
SIO_000300: 1.951768e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.11e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.66e-1

GenotypeQuality
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bin: 7.25e1
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
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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: 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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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
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: 10390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.235e1

VQSLOD
type: SiteQuality
SIO_000300: 4.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.951285e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.06e-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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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: 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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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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: 0
allele frequency: 0.0e0
allele num: 8642
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: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.622786759045419e-5
allele num: 10392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.115e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.598e0

DP
type: SiteQuality
SIO_000300: 1.95109e6

VQSLOD
type: SiteQuality
SIO_000300: 5.639999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.498e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.99e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501185936890143e-5
allele num: 66614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

Other
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num of homozygotes: 0

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

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

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

FS
type: SiteQuality
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DP
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MQRankSum
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MQ
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QD
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InbreedingCoeff
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ReadPosRankSum
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SIO_000300: -9.2e-2

ClippingRankSum
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SIO_000300: -2.48e-1

BaseQRankSum
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SIO_000300: 3.33e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e-2

GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

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

South Asian
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allele count: 2
allele frequency: 1.221896383186706e-4
allele num: 16368
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

QD
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MQ
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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VQSLOD
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FS
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MQRankSum
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DP
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

South Asian
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allele count: 5
allele frequency: 3.070875813782091e-4
allele num: 16282
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: 66562
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.979e1

FS
type: SiteQuality
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DP
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -3.73e-1

ReadPosRankSum
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

African
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: 1
allele frequency: 1.502584445245823e-5
allele num: 66552
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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BaseQRankSum
type: SiteQuality
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MQRankSum
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DP
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FS
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QD
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele num: 16174
num of homozygotes: 0

African
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

InbreedingCoeff
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SIO_000300: 7.6e-3

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

East Asian
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num of homozygotes: 0

European (Non-Finnish)
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African
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Latino
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European (Finnish)
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South Asian
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Other
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ReadPosRankSum
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DP
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MQ
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FS
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QD
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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East Asian
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African
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Latino
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European (Finnish)
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Other
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VQSLOD
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ReadPosRankSum
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DP
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QD
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FS
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MQ
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.040160520475481e-5
allele num: 65786
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
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: 14266
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.889128e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e0

FS
type: SiteQuality
SIO_000300: 1.2967e1

QD
type: SiteQuality
SIO_000300: 1.267e1

MQRankSum
type: SiteQuality
SIO_000300: 5.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.526e0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
type: Population
allele count: 1
allele frequency: 9.742790335151988e-5
allele num: 10264
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65756
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14208
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.54e-1

DP
type: SiteQuality
SIO_000300: 1.886863e6

FS
type: SiteQuality
SIO_000300: 1.0288e1

MQRankSum
type: SiteQuality
SIO_000300: -3.62e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 1.337e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.36e-1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.038288288288288e-5
allele num: 14208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65756
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.0288e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: 6.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

QD
type: SiteQuality
SIO_000300: 1.337e1

MQRankSum
type: SiteQuality
SIO_000300: -3.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.54e-1

DP
type: SiteQuality
SIO_000300: 1.886863e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 8505
bin: 9.75e1
variant carriers: 1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522209029743965e-5
allele num: 65694
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14034
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.811e0

MQRankSum
type: SiteQuality
SIO_000300: -5.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 7.525e0

MQ
type: SiteQuality
SIO_000300: 5.895e1

QD
type: SiteQuality
SIO_000300: 7.56e0

DP
type: SiteQuality
SIO_000300: 1.885143e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.07e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8502
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variant carriers: 2

GenotypeQuality
all individuals: 4520
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.045994517209869e-5
allele num: 65660
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14006
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

FS
type: SiteQuality
SIO_000300: 1.029e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.965e0

DP
type: SiteQuality
SIO_000300: 1.877811e6

VQSLOD
type: SiteQuality
SIO_000300: 2.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-1

QD
type: SiteQuality
SIO_000300: 1.28e1

GenotypeQuality
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variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524111443028714e-5
allele num: 65612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13846
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.685e-1

DP
type: SiteQuality
SIO_000300: 1.8718e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.84e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

MQ
type: SiteQuality
SIO_000300: 5.942e1

MQRankSum
type: SiteQuality
SIO_000300: 1.61e0

QD
type: SiteQuality
SIO_000300: 1.374e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.976e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6602
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East Asian
type: Population
allele count: 1
allele frequency: 1.172058134083451e-4
allele num: 8532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13606
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.953e1

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