http://identifiers.org/exac.variant/2-206608121-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608121
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608121
    reference: chr 2
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1486A>C
  hgvsp: ENSP00000349632.4:p.Lys496Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1486A>C
  hgvsp: ENSP00000350432.5:p.Lys496Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1486A>C
  hgvsp: ENSP00000387519.1:p.Lys496Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1486A>C
  hgvsp: ENSP00000353582.3:p.Lys496Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1486A>C
  hgvsp: ENSP00000439261.1:p.Lys496Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1486A>C
  hgvsp: ENSP00000439658.1:p.Lys496Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.391A>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1486A>C
  hgvsp: ENSP00000407626.2:p.Lys496Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1486A>C
  hgvsp: ENSP00000272849.3:p.Lys496Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1486A>C
  hgvsp: ENSP00000347238.4:p.Lys496Gln
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33837
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys496Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

2-206608125-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608125
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608125
    reference: chr 2
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1490C>T
  hgvsp: ENSP00000347238.4:p.Thr497Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1490C>T
  hgvsp: ENSP00000439261.1:p.Thr497Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.395C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1490C>T
  hgvsp: ENSP00000439658.1:p.Thr497Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1490C>T
  hgvsp: ENSP00000349632.4:p.Thr497Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1490C>T
  hgvsp: ENSP00000272849.3:p.Thr497Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1490C>T
  hgvsp: ENSP00000353582.3:p.Thr497Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1490C>T
  hgvsp: ENSP00000407626.2:p.Thr497Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1490C>T
  hgvsp: ENSP00000387519.1:p.Thr497Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1490C>T
  hgvsp: ENSP00000350432.5:p.Thr497Ile
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr497Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

2-206608129-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608129
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608129
    reference: chr 2
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1494G>A
  hgvsp: ENST00000417189.1:c.1494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1494G>A
  hgvsp: ENST00000360409.3:c.1494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1494G>A
  hgvsp: ENST00000355117.4:c.1494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1494G>A
  hgvsp: ENST00000357118.4:c.1494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1494G>A
  hgvsp: ENST00000412873.2:c.1494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1494G>A
  hgvsp: ENST00000357785.5:c.1494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1494G>A
  hgvsp: ENST00000272849.3:c.1494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1494G>A
  hgvsp: ENST00000540178.1:c.1494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1494G>A
  hgvsp: ENST00000540841.1:c.1494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.399G>A
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11605
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val498Val
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

2-206608129-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608129
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608128
    reference: chr 2
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1497delA
  hgvsp: ENSP00000353582.3:p.Gly500ValfsTer31
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1497delA
  hgvsp: ENSP00000439261.1:p.Gly500ValfsTer31
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1497delA
  hgvsp: ENSP00000407626.2:p.Gly500ValfsTer31
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.402delA
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1497delA
  hgvsp: ENSP00000387519.1:p.Gly500ValfsTer31
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1497delA
  hgvsp: ENSP00000350432.5:p.Gly500ValfsTer31
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1497delA
  hgvsp: ENSP00000347238.4:p.Gly500ValfsTer31
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1497delA
  hgvsp: ENSP00000272849.3:p.Gly500ValfsTer31
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1497delA
  hgvsp: ENSP00000439658.1:p.Gly500ValfsTer31
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1497delA
  hgvsp: ENSP00000349632.4:p.Gly500ValfsTer31
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly500ValfsTer31
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
reference allele: GA
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP

2-206608133-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608133
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608133
    reference: chr 2
allele count: 2
allele frequency: 1.647446457990115e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.403G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1498G>A
  hgvsp: ENSP00000407626.2:p.Gly500Ser
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1498G>A
  hgvsp: ENSP00000347238.4:p.Gly500Ser
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1498G>A
  hgvsp: ENSP00000439658.1:p.Gly500Ser
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1498G>A
  hgvsp: ENSP00000350432.5:p.Gly500Ser
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1498G>A
  hgvsp: ENSP00000272849.3:p.Gly500Ser
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1498G>A
  hgvsp: ENSP00000353582.3:p.Gly500Ser
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1498G>A
  hgvsp: ENSP00000439261.1:p.Gly500Ser
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1498G>A
  hgvsp: ENSP00000349632.4:p.Gly500Ser
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1498G>A
  hgvsp: ENSP00000387519.1:p.Gly500Ser
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33848
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly500Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

2-206608151-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608151
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608151
    reference: chr 2
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1516G>A
  hgvsp: ENSP00000439658.1:p.Ala506Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1516G>A
  hgvsp: ENSP00000387519.1:p.Ala506Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1516G>A
  hgvsp: ENSP00000353582.3:p.Ala506Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1516G>A
  hgvsp: ENSP00000347238.4:p.Ala506Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1516G>A
  hgvsp: ENSP00000407626.2:p.Ala506Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1516G>A
  hgvsp: ENSP00000350432.5:p.Ala506Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1516G>A
  hgvsp: ENSP00000272849.3:p.Ala506Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.421G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1516G>A
  hgvsp: ENSP00000349632.4:p.Ala506Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1516G>A
  hgvsp: ENSP00000439261.1:p.Ala506Thr
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12176
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala506Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

2-206608152-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608152
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608152
    reference: chr 2
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.422C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1517C>T
  hgvsp: ENSP00000272849.3:p.Ala506Val
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1517C>T
  hgvsp: ENSP00000439658.1:p.Ala506Val
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1517C>T
  hgvsp: ENSP00000407626.2:p.Ala506Val
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1517C>T
  hgvsp: ENSP00000353582.3:p.Ala506Val
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1517C>T
  hgvsp: ENSP00000347238.4:p.Ala506Val
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1517C>T
  hgvsp: ENSP00000349632.4:p.Ala506Val
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1517C>T
  hgvsp: ENSP00000387519.1:p.Ala506Val
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1517C>T
  hgvsp: ENSP00000350432.5:p.Ala506Val
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1517C>T
  hgvsp: ENSP00000439261.1:p.Ala506Val
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala506Val
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: QD

2-206608154-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608154
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608154
    reference: chr 2
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1519C>T
  hgvsp: ENSP00000272849.3:p.Arg507Cys
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1519C>T
  hgvsp: ENSP00000439658.1:p.Arg507Cys
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1519C>T
  hgvsp: ENSP00000387519.1:p.Arg507Cys
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1519C>T
  hgvsp: ENSP00000353582.3:p.Arg507Cys
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1519C>T
  hgvsp: ENSP00000349632.4:p.Arg507Cys
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1519C>T
  hgvsp: ENSP00000439261.1:p.Arg507Cys
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1519C>T
  hgvsp: ENSP00000350432.5:p.Arg507Cys
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1519C>T
  hgvsp: ENSP00000407626.2:p.Arg507Cys
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1519C>T
  hgvsp: ENSP00000347238.4:p.Arg507Cys
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.424C>T
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg507Cys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

2-206608155-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608155
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608155
    reference: chr 2
allele count: 13
allele frequency: 1.070893124866138e-4
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1520G>A
  hgvsp: ENSP00000353582.3:p.Arg507His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1520G>A
  hgvsp: ENSP00000439261.1:p.Arg507His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1520G>A
  hgvsp: ENSP00000387519.1:p.Arg507His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.425G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1520G>A
  hgvsp: ENSP00000349632.4:p.Arg507His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1520G>A
  hgvsp: ENSP00000272849.3:p.Arg507His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1520G>A
  hgvsp: ENSP00000407626.2:p.Arg507His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1520G>A
  hgvsp: ENSP00000347238.4:p.Arg507His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1520G>A
  hgvsp: ENSP00000350432.5:p.Arg507His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1520G>A
  hgvsp: ENSP00000439658.1:p.Arg507His
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12178
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg507His
num of homozygotes: 1
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

2-206608156-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608156
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608156
    reference: chr 2
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1521C>T
  hgvsp: ENST00000540841.1:c.1521C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1521C>T
  hgvsp: ENST00000357118.4:c.1521C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1521C>T
  hgvsp: ENST00000355117.4:c.1521C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.426C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1521C>T
  hgvsp: ENST00000412873.2:c.1521C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1521C>T
  hgvsp: ENST00000417189.1:c.1521C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1521C>T
  hgvsp: ENST00000360409.3:c.1521C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1521C>T
  hgvsp: ENST00000272849.3:c.1521C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1521C>T
  hgvsp: ENST00000540178.1:c.1521C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1521C>T
  hgvsp: ENST00000357785.5:c.1521C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11624
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg507Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

2-206608157-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608157
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608157
    reference: chr 2
allele count: 43
allele frequency: 3.542301672295906e-4
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1522G>A
  hgvsp: ENSP00000272849.3:p.Gly508Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1522G>A
  hgvsp: ENSP00000353582.3:p.Gly508Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1522G>A
  hgvsp: ENSP00000439261.1:p.Gly508Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1522G>A
  hgvsp: ENSP00000349632.4:p.Gly508Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1522G>A
  hgvsp: ENSP00000387519.1:p.Gly508Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1522G>A
  hgvsp: ENSP00000407626.2:p.Gly508Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1522G>A
  hgvsp: ENSP00000439658.1:p.Gly508Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1522G>A
  hgvsp: ENSP00000347238.4:p.Gly508Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1522G>A
  hgvsp: ENSP00000350432.5:p.Gly508Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.427G>A
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly508Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

2-206608157-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608157
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608157
    reference: chr 2
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1522G>T
  hgvsp: ENSP00000272849.3:p.Gly508Ter
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1522G>T
  hgvsp: ENSP00000350432.5:p.Gly508Ter
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1522G>T
  hgvsp: ENSP00000353582.3:p.Gly508Ter
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1522G>T
  hgvsp: ENSP00000439261.1:p.Gly508Ter
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1522G>T
  hgvsp: ENSP00000349632.4:p.Gly508Ter
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.427G>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1522G>T
  hgvsp: ENSP00000347238.4:p.Gly508Ter
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1522G>T
  hgvsp: ENSP00000407626.2:p.Gly508Ter
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1522G>T
  hgvsp: ENSP00000439658.1:p.Gly508Ter
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1522G>T
  hgvsp: ENSP00000387519.1:p.Gly508Ter
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly508Ter
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

2-206608190-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608190
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608190
    reference: chr 2
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1555G>A
  hgvsp: ENSP00000347238.4:p.Ala519Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1555G>A
  hgvsp: ENSP00000439261.1:p.Ala519Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1555G>A
  hgvsp: ENSP00000439658.1:p.Ala519Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1555G>A
  hgvsp: ENSP00000349632.4:p.Ala519Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.460G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1555G>A
  hgvsp: ENSP00000407626.2:p.Ala519Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1555G>A
  hgvsp: ENSP00000272849.3:p.Ala519Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1555G>A
  hgvsp: ENSP00000387519.1:p.Ala519Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1555G>A
  hgvsp: ENSP00000350432.5:p.Ala519Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1555G>A
  hgvsp: ENSP00000353582.3:p.Ala519Thr
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala519Thr
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

2-206608196-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608196
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608196
    reference: chr 2
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1561G>T
  hgvsp: ENSP00000439261.1:p.Val521Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1561G>T
  hgvsp: ENSP00000347238.4:p.Val521Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.466G>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1561G>T
  hgvsp: ENSP00000353582.3:p.Val521Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1561G>T
  hgvsp: ENSP00000407626.2:p.Val521Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1561G>T
  hgvsp: ENSP00000387519.1:p.Val521Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1561G>T
  hgvsp: ENSP00000439658.1:p.Val521Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1561G>T
  hgvsp: ENSP00000272849.3:p.Val521Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1561G>T
  hgvsp: ENSP00000350432.5:p.Val521Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1561G>T
  hgvsp: ENSP00000349632.4:p.Val521Leu
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33914
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val521Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

2-206608198-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608198
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608198
    reference: chr 2
allele count: 36
allele frequency: 2.965941109591524e-4
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1563G>A
  hgvsp: ENST00000357785.5:c.1563G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1563G>A
  hgvsp: ENST00000540841.1:c.1563G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1563G>A
  hgvsp: ENST00000272849.3:c.1563G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1563G>A
  hgvsp: ENST00000355117.4:c.1563G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1563G>A
  hgvsp: ENST00000540178.1:c.1563G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1563G>A
  hgvsp: ENST00000357118.4:c.1563G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1563G>A
  hgvsp: ENST00000360409.3:c.1563G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1563G>A
  hgvsp: ENST00000417189.1:c.1563G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1563G>A
  hgvsp: ENST00000412873.2:c.1563G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.468G>A
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val521Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

2-206608200-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608200
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608200
    reference: chr 2
allele count: 4
allele frequency: 3.295653033648617e-5
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1565G>A
  hgvsp: ENSP00000387519.1:p.Arg522His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1565G>A
  hgvsp: ENSP00000349632.4:p.Arg522His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.470G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1565G>A
  hgvsp: ENSP00000353582.3:p.Arg522His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1565G>A
  hgvsp: ENSP00000272849.3:p.Arg522His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1565G>A
  hgvsp: ENSP00000350432.5:p.Arg522His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1565G>A
  hgvsp: ENSP00000407626.2:p.Arg522His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1565G>A
  hgvsp: ENSP00000439261.1:p.Arg522His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1565G>A
  hgvsp: ENSP00000439658.1:p.Arg522His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1565G>A
  hgvsp: ENSP00000347238.4:p.Arg522His
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg522His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

2-206608217-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608217
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608217
    reference: chr 2
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1582T>C
  hgvsp: ENSP00000353582.3:p.Tyr528His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1582T>C
  hgvsp: ENSP00000349632.4:p.Tyr528His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1582T>C
  hgvsp: ENSP00000439658.1:p.Tyr528His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1582T>C
  hgvsp: ENSP00000439261.1:p.Tyr528His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1582T>C
  hgvsp: ENSP00000350432.5:p.Tyr528His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1582T>C
  hgvsp: ENSP00000407626.2:p.Tyr528His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1582T>C
  hgvsp: ENSP00000347238.4:p.Tyr528His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1582T>C
  hgvsp: ENSP00000272849.3:p.Tyr528His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.487T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1582T>C
  hgvsp: ENSP00000387519.1:p.Tyr528His
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Tyr528His
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD

2-206608228-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608228
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608228
    reference: chr 2
allele count: 4
allele frequency: 3.298479400996141e-5
allele num: 121268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1593C>T
  hgvsp: ENST00000540841.1:c.1593C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.498C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1593C>T
  hgvsp: ENST00000272849.3:c.1593C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1593C>T
  hgvsp: ENST00000357118.4:c.1593C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1593C>T
  hgvsp: ENST00000417189.1:c.1593C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1593C>T
  hgvsp: ENST00000357785.5:c.1593C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1593C>T
  hgvsp: ENST00000360409.3:c.1593C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1593C>T
  hgvsp: ENST00000412873.2:c.1593C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1593C>T
  hgvsp: ENST00000540178.1:c.1593C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1593C>T
  hgvsp: ENST00000355117.4:c.1593C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn531Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

2-206608229-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608229
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608229
    reference: chr 2
allele count: 9
allele frequency: 7.423292642692181e-5
allele num: 121240
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1594G>A
  hgvsp: ENSP00000387519.1:p.Gly532Ser
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1594G>A
  hgvsp: ENSP00000439658.1:p.Gly532Ser
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1594G>A
  hgvsp: ENSP00000407626.2:p.Gly532Ser
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1594G>A
  hgvsp: ENSP00000350432.5:p.Gly532Ser
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1594G>A
  hgvsp: ENSP00000272849.3:p.Gly532Ser
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1594G>A
  hgvsp: ENSP00000347238.4:p.Gly532Ser
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1594G>A
  hgvsp: ENSP00000353582.3:p.Gly532Ser
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.499G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1594G>A
  hgvsp: ENSP00000349632.4:p.Gly532Ser
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1594G>A
  hgvsp: ENSP00000439261.1:p.Gly532Ser
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33856
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly532Ser
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

2-206608233-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608233
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608233
    reference: chr 2
allele count: 3
allele frequency: 2.475002475002475e-5
allele num: 121212
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1598A>G
  hgvsp: ENSP00000353582.3:p.Lys533Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1598A>G
  hgvsp: ENSP00000347238.4:p.Lys533Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1598A>G
  hgvsp: ENSP00000387519.1:p.Lys533Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1598A>G
  hgvsp: ENSP00000350432.5:p.Lys533Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1598A>G
  hgvsp: ENSP00000439658.1:p.Lys533Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1598A>G
  hgvsp: ENSP00000272849.3:p.Lys533Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1598A>G
  hgvsp: ENSP00000439261.1:p.Lys533Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1598A>G
  hgvsp: ENSP00000349632.4:p.Lys533Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1598A>G
  hgvsp: ENSP00000407626.2:p.Lys533Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.503A>G
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys533Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

2-206608241-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608241
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608241
    reference: chr 2
allele count: 1
allele frequency: 8.260503229856763e-6
allele num: 121058
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.511G>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1606G>C
  hgvsp: ENSP00000439658.1:p.Glu536Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1606G>C
  hgvsp: ENSP00000347238.4:p.Glu536Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1606G>C
  hgvsp: ENSP00000353582.3:p.Glu536Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1606G>C
  hgvsp: ENSP00000387519.1:p.Glu536Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1606G>C
  hgvsp: ENSP00000349632.4:p.Glu536Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1606G>C
  hgvsp: ENSP00000272849.3:p.Glu536Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1606G>C
  hgvsp: ENSP00000439261.1:p.Glu536Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1606G>C
  hgvsp: ENSP00000407626.2:p.Glu536Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1606G>C
  hgvsp: ENSP00000350432.5:p.Glu536Gln
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu536Gln
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

2-206608242-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608242
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608242
    reference: chr 2
allele count: 3
allele frequency: 2.478806206930742e-5
allele num: 121026
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1607A>G
  hgvsp: ENSP00000349632.4:p.Glu536Gly
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1607A>G
  hgvsp: ENSP00000272849.3:p.Glu536Gly
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1607A>G
  hgvsp: ENSP00000350432.5:p.Glu536Gly
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1607A>G
  hgvsp: ENSP00000347238.4:p.Glu536Gly
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1607A>G
  hgvsp: ENSP00000407626.2:p.Glu536Gly
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1607A>G
  hgvsp: ENSP00000353582.3:p.Glu536Gly
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.512A>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1607A>G
  hgvsp: ENSP00000439658.1:p.Glu536Gly
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1607A>G
  hgvsp: ENSP00000387519.1:p.Glu536Gly
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1607A>G
  hgvsp: ENSP00000439261.1:p.Glu536Gly
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11989
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11708
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu536Gly
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

2-206608248-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608248
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608248
    reference: chr 2
allele count: 1
allele frequency: 8.274446853227862e-6
allele num: 120854
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1613T>C
  hgvsp: ENSP00000349632.4:p.Ile538Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1613T>C
  hgvsp: ENSP00000407626.2:p.Ile538Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1613T>C
  hgvsp: ENSP00000350432.5:p.Ile538Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1613T>C
  hgvsp: ENSP00000347238.4:p.Ile538Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1613T>C
  hgvsp: ENSP00000439658.1:p.Ile538Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1613T>C
  hgvsp: ENSP00000272849.3:p.Ile538Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1613T>C
  hgvsp: ENSP00000439261.1:p.Ile538Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1613T>C
  hgvsp: ENSP00000353582.3:p.Ile538Thr
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.518T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1613T>C
  hgvsp: ENSP00000387519.1:p.Ile538Thr
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile538Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD

2-206608251-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608251
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608251
    reference: chr 2
allele count: 1
allele frequency: 8.296138976920141e-6
allele num: 120538
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1616A>G
  hgvsp: ENSP00000272849.3:p.Gln539Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1616A>G
  hgvsp: ENSP00000349632.4:p.Gln539Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1616A>G
  hgvsp: ENSP00000439658.1:p.Gln539Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1616A>G
  hgvsp: ENSP00000353582.3:p.Gln539Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.521A>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1616A>G
  hgvsp: ENSP00000350432.5:p.Gln539Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1616A>G
  hgvsp: ENSP00000407626.2:p.Gln539Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1616A>G
  hgvsp: ENSP00000347238.4:p.Gln539Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1616A>G
  hgvsp: ENSP00000387519.1:p.Gln539Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1616A>G
  hgvsp: ENSP00000439261.1:p.Gln539Arg
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln539Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

2-206608266-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608266
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608266
    reference: chr 2
allele count: 1
allele frequency: 8.35282325425994e-6
allele num: 119720
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1631A>G
  hgvsp: ENSP00000439658.1:p.Gln544Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1631A>G
  hgvsp: ENSP00000407626.2:p.Gln544Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1631A>G
  hgvsp: ENSP00000349632.4:p.Gln544Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1631A>G
  hgvsp: ENSP00000347238.4:p.Gln544Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1631A>G
  hgvsp: ENSP00000272849.3:p.Gln544Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1631A>G
  hgvsp: ENSP00000350432.5:p.Gln544Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1631A>G
  hgvsp: ENSP00000439261.1:p.Gln544Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1631A>G
  hgvsp: ENSP00000387519.1:p.Gln544Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1631A>G
  hgvsp: ENSP00000353582.3:p.Gln544Arg
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.536A>G
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11312
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1040
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gln544Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

2-206608278-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608278
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608278
    reference: chr 2
allele count: 1
allele frequency: 8.529075618784437e-6
allele num: 117246
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1641+2T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1641+2T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1643T>C
  hgvsp: ENSP00000347238.4:p.Val548Ala
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.548T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1641+2T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1641+2T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1641+2T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1643T>C
  hgvsp: ENSP00000387519.1:p.Val548Ala
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1641+2T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1641+2T>C
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31054
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10315
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 8.25e1
  variant carriers: 0
hgvs: c.1641+2T>C
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

2-206608282-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608282
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608282
    reference: chr 2
allele count: 2
allele frequency: 1.724494723046147e-5
allele num: 115976
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1641+6C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.552C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1641+6C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1641+6C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1647C>T
  hgvsp: ENST00000355117.4:c.1647C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1641+6C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1641+6C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1647C>T
  hgvsp: ENST00000417189.1:c.1647C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1641+6C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1641+6C>T
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9695
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
hgvs: c.1641+6C>T
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

2-206608300-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608300
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608300
    reference: chr 2
allele count: 4
allele frequency: 3.796218965909954e-5
allele num: 105368
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1641+24G>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1641+24G>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1641+24G>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1641+24G>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.570G>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.1665G>T
  hgvsp: ENST00000417189.1:c.1665G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1641+24G>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1641+24G>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.1665G>T
  hgvsp: ENST00000355117.4:c.1665G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1641+24G>T
  variant of: http://identifiers.org/hgnc/8005
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10798
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3674
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2647
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu555Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

2-206608304-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608304
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608304
    reference: chr 2
allele count: 30
allele frequency: 2.917096128041073e-4
allele num: 102842
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1641+28C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.*1C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1641+28C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1641+28C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.*1C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1641+28C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.574C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1641+28C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1641+28C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1641+28C>T
  variant of: http://identifiers.org/hgnc/8005
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17489
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14745
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8608
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10235
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3226
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

2-206608305-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608305
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608305
    reference: chr 2
allele count: 2
allele frequency: 1.959055735135665e-5
allele num: 102090
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1641+29G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1641+29G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.*2G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1641+29G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.*2G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1641+29G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.575G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1641+29G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1641+29G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1641+29G>A
  variant of: http://identifiers.org/hgnc/8005
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8925
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15520
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16706
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18367
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

2-206608315-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608315
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608315
    reference: chr 2
allele count: 1
allele frequency: 1.041601566568756e-5
allele num: 96006
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1641+39A>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1641+39A>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1641+39A>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1641+39A>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1641+39A>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.585A>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1641+39A>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1641+39A>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.*12A>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.*12A>G
  variant of: http://identifiers.org/hgnc/8005
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21509
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7639
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22917
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

2-206608317-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608317
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608316
    reference: chr 2
allele count: 1
allele frequency: 1.065666361175643e-5
allele num: 93838
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1641+44delG
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.590delG
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1641+44delG
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.*17delG
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1641+44delG
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1641+44delG
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.*17delG
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1641+44delG
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1641+44delG
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1641+44delG
  variant of: http://identifiers.org/hgnc/8005
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5763
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8370
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12153
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1842
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 932
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23398
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: AG
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

2-206608328-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608328
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608328
    reference: chr 2
allele count: 1
allele frequency: 1.129815840018077e-5
allele num: 88510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1641+52G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1641+52G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.*25G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.*25G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1641+52G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.598G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1641+52G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1641+52G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1641+52G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1641+52G>A
  variant of: http://identifiers.org/hgnc/8005
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4951
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24893
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7564
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23542
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1039
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3002
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD

2-206608329-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608329
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608329
    reference: chr 2
allele count: 1
allele frequency: 1.130480001808768e-5
allele num: 88458
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1641+53T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1641+53T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1641+53T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.*26T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.*26T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1641+53T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.599T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1641+53T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1641+53T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1641+53T>C
  variant of: http://identifiers.org/hgnc/8005
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24889
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7516
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6220
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

2-206608336-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608336
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608336
    reference: chr 2
allele count: 4
allele frequency: 4.784345621127671e-5
allele num: 83606
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1641+60C>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.*33C>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.*33C>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1641+60C>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.606C>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1641+60C>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1641+60C>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1641+60C>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1641+60C>G
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1641+60C>G
  variant of: http://identifiers.org/hgnc/8005
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23982
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14683
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4704
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3988
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

2-206608336-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608336
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608336
    reference: chr 2
allele count: 2
allele frequency: 2.392172810563835e-5
allele num: 83606
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1641+60C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1641+60C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.606C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.*33C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1641+60C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1641+60C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1641+60C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.*33C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1641+60C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1641+60C>T
  variant of: http://identifiers.org/hgnc/8005
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14683
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23982
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4704
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5511
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ

2-206608339-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608339
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608339
    reference: chr 2
allele count: 1
allele frequency: 1.220166918834497e-5
allele num: 81956
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.*36G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1641+63G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1641+63G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1641+63G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1641+63G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.609G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1641+63G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.*36G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1641+63G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1641+63G>A
  variant of: http://identifiers.org/hgnc/8005
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9740
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23436
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21190
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4834
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD

2-206608349-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206608349
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206608349
    reference: chr 2
allele count: 2
allele frequency: 2.643055372010044e-5
allele num: 75670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1641+73C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000387519
  ensembl transcript: ENST00000417189
  gene symbol: NRP2
  hgvsc: ENST00000417189.1:c.*46C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1641+73C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1641+73C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1641+73C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1641+73C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118257
  ensembl transcript: ENST00000478054
  gene symbol: NRP2
  hgvsc: ENST00000478054.1:n.619C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1641+73C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000347238
  ensembl transcript: ENST00000355117
  gene symbol: NRP2
  hgvsc: ENST00000355117.4:c.*46C>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1641+73C>T
  variant of: http://identifiers.org/hgnc/8005
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18035
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21076
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9930
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3267
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1797
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

2-206610419-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610419
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610419
    reference: chr 2
allele count: 1
allele frequency: 8.360924383799873e-6
allele num: 119604
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1642-51A>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1642-51A>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1642-51A>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1642-51A>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1642-51A>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1642-51A>T
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1642-51A>T
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3977
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7162
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11025
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6108
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10232
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3180
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13238
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3974
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3459
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1218
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-206610425-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610425
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610425
    reference: chr 2
allele count: 1
allele frequency: 8.357430591538938e-6
allele num: 119654
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1642-45A>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1642-45A>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1642-45A>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1642-45A>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1642-45A>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1642-45A>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1642-45A>C
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11161
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7785
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2483
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2976
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1126
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6130
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2609
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1642
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2993
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

2-206610443-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610443
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610442
    reference: chr 2
allele count: 1
allele frequency: 8.34153584357952e-6
allele num: 119882
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1642-24delG
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1642-24delG
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1642-24delG
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1642-24delG
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1642-24delG
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1642-24delG
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1642-24delG
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7959
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6558
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2029
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1605
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3213
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4072
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1387
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18310
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: AG
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ

2-206610451-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610451
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610451
    reference: chr 2
allele count: 2
allele frequency: 1.666305633779348e-5
allele num: 120026
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1642-19G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1642-19G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1642-19G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1642-19G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1642-19G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1642-19G>A
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1642-19G>A
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17963
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8240
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4202
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1320
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3358
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 893
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13283
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1595
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18639
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6751
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

2-206610452-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610452
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610452
    reference: chr 2
allele count: 1
allele frequency: 8.333472224537076e-6
allele num: 119998
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1642-18T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1642-18T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1642-18T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1642-18T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1642-18T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1642-18T>C
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1642-18T>C
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18700
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3314
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2066
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 880
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1257
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

2-206610475-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610475
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610475
    reference: chr 2
allele count: 1
allele frequency: 8.293386853323161e-6
allele num: 120578
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1647C>T
  hgvsp: ENST00000360409.3:c.1647C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1647C>T
  hgvsp: ENST00000540178.1:c.1647C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1647C>T
  hgvsp: ENST00000412873.2:c.1647C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1647C>T
  hgvsp: ENST00000357118.4:c.1647C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1647C>T
  hgvsp: ENST00000272849.3:c.1647C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1647C>T
  hgvsp: ENST00000357785.5:c.1647C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1647C>T
  hgvsp: ENST00000540841.1:c.1647C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2144
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4615
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Phe549Phe
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

2-206610485-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610485
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610485
    reference: chr 2
allele count: 1
allele frequency: 8.276638360563474e-6
allele num: 120822
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1657A>T
  hgvsp: ENSP00000349632.4:p.Met553Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1657A>T
  hgvsp: ENSP00000353582.3:p.Met553Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1657A>T
  hgvsp: ENSP00000272849.3:p.Met553Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1657A>T
  hgvsp: ENSP00000439261.1:p.Met553Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1657A>T
  hgvsp: ENSP00000407626.2:p.Met553Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1657A>T
  hgvsp: ENSP00000439658.1:p.Met553Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1657A>T
  hgvsp: ENSP00000350432.5:p.Met553Leu
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18635
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2171
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21217
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4761
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13363
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met553Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

2-206610487-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610487
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610487
    reference: chr 2
allele count: 1
allele frequency: 8.274857672448034e-6
allele num: 120848
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1659G>A
  hgvsp: ENSP00000439658.1:p.Met553Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1659G>A
  hgvsp: ENSP00000350432.5:p.Met553Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1659G>A
  hgvsp: ENSP00000349632.4:p.Met553Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1659G>A
  hgvsp: ENSP00000439261.1:p.Met553Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1659G>A
  hgvsp: ENSP00000353582.3:p.Met553Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1659G>A
  hgvsp: ENSP00000407626.2:p.Met553Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1659G>A
  hgvsp: ENSP00000272849.3:p.Met553Ile
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4302
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4768
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7539
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3745
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Met553Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

2-206610487-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610487
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610487
    reference: chr 2
allele count: 1
allele frequency: 8.274857672448034e-6
allele num: 120848
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1659G>T
  hgvsp: ENSP00000353582.3:p.Met553Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1659G>T
  hgvsp: ENSP00000272849.3:p.Met553Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1659G>T
  hgvsp: ENSP00000350432.5:p.Met553Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1659G>T
  hgvsp: ENSP00000407626.2:p.Met553Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1659G>T
  hgvsp: ENSP00000439658.1:p.Met553Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1659G>T
  hgvsp: ENSP00000349632.4:p.Met553Ile
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1659G>T
  hgvsp: ENSP00000439261.1:p.Met553Ile
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3757
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7539
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21275
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met553Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

2-206610501-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610501
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610501
    reference: chr 2
allele count: 1
allele frequency: 8.266375690242371e-6
allele num: 120972
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1673C>T
  hgvsp: ENSP00000439261.1:p.Pro558Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1673C>T
  hgvsp: ENSP00000349632.4:p.Pro558Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1673C>T
  hgvsp: ENSP00000272849.3:p.Pro558Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1673C>T
  hgvsp: ENSP00000350432.5:p.Pro558Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1673C>T
  hgvsp: ENSP00000353582.3:p.Pro558Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1673C>T
  hgvsp: ENSP00000407626.2:p.Pro558Leu
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1673C>T
  hgvsp: ENSP00000439658.1:p.Pro558Leu
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18236
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2203
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21320
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7696
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro558Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

2-206610502-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610502
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610502
    reference: chr 2
allele count: 1
allele frequency: 8.26541913940456e-6
allele num: 120986
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1674T>A
  hgvsp: ENST00000360409.3:c.1674T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1674T>A
  hgvsp: ENST00000272849.3:c.1674T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1674T>A
  hgvsp: ENST00000357785.5:c.1674T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1674T>A
  hgvsp: ENST00000412873.2:c.1674T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1674T>A
  hgvsp: ENST00000540841.1:c.1674T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1674T>A
  hgvsp: ENST00000357118.4:c.1674T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1674T>A
  hgvsp: ENST00000540178.1:c.1674T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4040
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28004
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2651
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro558Pro
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

2-206610502-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610502
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610502
    reference: chr 2
allele count: 22520
allele frequency: 1.861372390193907e-1
allele num: 120986
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1674T>G
  hgvsp: ENST00000357785.5:c.1674T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1674T>G
  hgvsp: ENST00000412873.2:c.1674T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1674T>G
  hgvsp: ENST00000360409.3:c.1674T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1674T>G
  hgvsp: ENST00000272849.3:c.1674T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1674T>G
  hgvsp: ENST00000540841.1:c.1674T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1674T>G
  hgvsp: ENST00000540178.1:c.1674T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1674T>G
  hgvsp: ENST00000357118.4:c.1674T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 4.75e1
  variant carriers: 2250
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 5.75e1
  variant carriers: 1393
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 6.75e1
  variant carriers: 640
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.75e1
  variant carriers: 242
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 7.25e1
  variant carriers: 451
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 5.25e1
  variant carriers: 1760
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 8.25e1
  variant carriers: 212
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 4.25e1
  variant carriers: 2419
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 9.25e1
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 6.25e1
  variant carriers: 913
genotype depth: GenotypeDepth
  all individuals: 12558
  bin: 2.25e1
  variant carriers: 704
genotype depth: GenotypeDepth
  all individuals: 5359
  bin: 3.75e1
  variant carriers: 2303
genotype depth: GenotypeDepth
  all individuals: 8503
  bin: 3.25e1
  variant carriers: 1921
genotype depth: GenotypeDepth
  all individuals: 11741
  bin: 2.75e1
  variant carriers: 1308
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 7.75e1
  variant carriers: 301
genotype depth: GenotypeDepth
  all individuals: 4040
  bin: 9.75e1
  variant carriers: 2822
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 8.75e1
  variant carriers: 167
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2637
  bin: 7.25e1
  variant carriers: 65
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 5172
  bin: 6.75e1
  variant carriers: 69
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 2.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 2651
  bin: 8.25e1
  variant carriers: 86
genotype quality: GenotypeQuality
  all individuals: 14571
  bin: 6.25e1
  variant carriers: 62
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 4.75e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.75e1
  variant carriers: 8
hgvs: p.Pro558Pro
num of homozygotes: 2539
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

2-206610509-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610509
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610509
    reference: chr 2
allele count: 1
allele frequency: 8.255456856982466e-6
allele num: 121132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1681C>T
  hgvsp: ENSP00000272849.3:p.Arg561Ter
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1681C>T
  hgvsp: ENSP00000349632.4:p.Arg561Ter
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1681C>T
  hgvsp: ENSP00000353582.3:p.Arg561Ter
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1681C>T
  hgvsp: ENSP00000439658.1:p.Arg561Ter
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1681C>T
  hgvsp: ENSP00000350432.5:p.Arg561Ter
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1681C>T
  hgvsp: ENSP00000439261.1:p.Arg561Ter
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1681C>T
  hgvsp: ENSP00000407626.2:p.Arg561Ter
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9696
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3553
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3945
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4663
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1975
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg561Ter
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

2-206610510-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610510
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610510
    reference: chr 2
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1682G>A
  hgvsp: ENSP00000350432.5:p.Arg561Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1682G>A
  hgvsp: ENSP00000353582.3:p.Arg561Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1682G>A
  hgvsp: ENSP00000439658.1:p.Arg561Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1682G>A
  hgvsp: ENSP00000349632.4:p.Arg561Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1682G>A
  hgvsp: ENSP00000407626.2:p.Arg561Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1682G>A
  hgvsp: ENSP00000272849.3:p.Arg561Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1682G>A
  hgvsp: ENSP00000439261.1:p.Arg561Gln
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3949
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17947
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg561Gln
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

2-206610513-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610513
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610513
    reference: chr 2
allele count: 3
allele frequency: 2.475492623031983e-5
allele num: 121188
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1685G>A
  hgvsp: ENSP00000272849.3:p.Arg562Lys
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1685G>A
  hgvsp: ENSP00000350432.5:p.Arg562Lys
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1685G>A
  hgvsp: ENSP00000439658.1:p.Arg562Lys
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1685G>A
  hgvsp: ENSP00000407626.2:p.Arg562Lys
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1685G>A
  hgvsp: ENSP00000349632.4:p.Arg562Lys
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1685G>A
  hgvsp: ENSP00000439261.1:p.Arg562Lys
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1685G>A
  hgvsp: ENSP00000353582.3:p.Arg562Lys
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2772
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13509
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17947
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4665
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg562Lys
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

2-206610519-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610519
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610519
    reference: chr 2
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1691A>G
  hgvsp: ENSP00000350432.5:p.Asp564Gly
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1691A>G
  hgvsp: ENSP00000407626.2:p.Asp564Gly
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1691A>G
  hgvsp: ENSP00000439261.1:p.Asp564Gly
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1691A>G
  hgvsp: ENSP00000439658.1:p.Asp564Gly
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1691A>G
  hgvsp: ENSP00000353582.3:p.Asp564Gly
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1691A>G
  hgvsp: ENSP00000272849.3:p.Asp564Gly
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1691A>G
  hgvsp: ENSP00000349632.4:p.Asp564Gly
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3576
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2762
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6849
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp564Gly
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

2-206610524-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610524
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610525
    reference: chr 2
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1698dupT
  hgvsp: ENSP00000439261.1:p.Pro567SerfsTer27
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1698dupT
  hgvsp: ENSP00000353582.3:p.Pro567SerfsTer27
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1698dupT
  hgvsp: ENSP00000349632.4:p.Pro567SerfsTer27
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1698dupT
  hgvsp: ENSP00000350432.5:p.Pro567SerfsTer27
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1698dupT
  hgvsp: ENSP00000407626.2:p.Pro567SerfsTer27
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1698dupT
  hgvsp: ENSP00000272849.3:p.Pro567SerfsTer27
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1698dupT
  hgvsp: ENSP00000439658.1:p.Pro567SerfsTer27
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17755
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro567SerfsTer27
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

2-206610526-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610526
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610526
    reference: chr 2
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1698T>G
  hgvsp: ENSP00000350432.5:p.Ile566Met
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1698T>G
  hgvsp: ENSP00000439658.1:p.Ile566Met
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1698T>G
  hgvsp: ENSP00000353582.3:p.Ile566Met
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1698T>G
  hgvsp: ENSP00000439261.1:p.Ile566Met
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1698T>G
  hgvsp: ENSP00000272849.3:p.Ile566Met
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1698T>G
  hgvsp: ENSP00000407626.2:p.Ile566Met
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1698T>G
  hgvsp: ENSP00000349632.4:p.Ile566Met
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13618
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3579
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3957
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6872
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile566Met
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

2-206610529-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610529
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610529
    reference: chr 2
allele count: 2
allele frequency: 1.649783878311941e-5
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1701G>A
  hgvsp: ENST00000360409.3:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1701G>A
  hgvsp: ENST00000357785.5:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1701G>A
  hgvsp: ENST00000357118.4:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1701G>A
  hgvsp: ENST00000412873.2:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1701G>A
  hgvsp: ENST00000540841.1:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1701G>A
  hgvsp: ENST00000540178.1:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1701G>A
  hgvsp: ENST00000272849.3:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13685
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9804
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1978
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro567Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/2-206610533-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610533
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610532
    reference: chr 2
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1706delA
  hgvsp: ENSP00000349632.4:p.Gln569ArgfsTer33
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1706delA
  hgvsp: ENSP00000353582.3:p.Gln569ArgfsTer33
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1706delA
  hgvsp: ENSP00000407626.2:p.Gln569ArgfsTer33
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1706delA
  hgvsp: ENSP00000439658.1:p.Gln569ArgfsTer33
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1706delA
  hgvsp: ENSP00000272849.3:p.Gln569ArgfsTer33
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1706delA
  hgvsp: ENSP00000350432.5:p.Gln569ArgfsTer33
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1706delA
  hgvsp: ENSP00000439261.1:p.Gln569ArgfsTer33
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9841
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6919
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3969
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17929
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3580
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17948
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gln569ArgfsTer33
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: CA
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD

2-206610535-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610535
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610535
    reference: chr 2
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1707G>C
  hgvsp: ENSP00000439658.1:p.Gln569His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1707G>C
  hgvsp: ENSP00000353582.3:p.Gln569His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1707G>C
  hgvsp: ENSP00000407626.2:p.Gln569His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1707G>C
  hgvsp: ENSP00000272849.3:p.Gln569His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1707G>C
  hgvsp: ENSP00000350432.5:p.Gln569His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1707G>C
  hgvsp: ENSP00000349632.4:p.Gln569His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1707G>C
  hgvsp: ENSP00000439261.1:p.Gln569His
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2766
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4678
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3967
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1979
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln569His
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

2-206610536-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610536
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610536
    reference: chr 2
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1708T>C
  hgvsp: ENSP00000349632.4:p.Tyr570His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1708T>C
  hgvsp: ENSP00000439261.1:p.Tyr570His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1708T>C
  hgvsp: ENSP00000353582.3:p.Tyr570His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1708T>C
  hgvsp: ENSP00000439658.1:p.Tyr570His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1708T>C
  hgvsp: ENSP00000407626.2:p.Tyr570His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1708T>C
  hgvsp: ENSP00000350432.5:p.Tyr570His
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1708T>C
  hgvsp: ENSP00000272849.3:p.Tyr570His
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17726
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6895
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2766
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr570His
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum

2-206610543-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610543
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610543
    reference: chr 2
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1715G>A
  hgvsp: ENSP00000349632.4:p.Arg572Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1715G>A
  hgvsp: ENSP00000407626.2:p.Arg572Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1715G>A
  hgvsp: ENSP00000350432.5:p.Arg572Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1715G>A
  hgvsp: ENSP00000272849.3:p.Arg572Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1715G>A
  hgvsp: ENSP00000353582.3:p.Arg572Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1715G>A
  hgvsp: ENSP00000439261.1:p.Arg572Gln
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1715G>A
  hgvsp: ENSP00000439658.1:p.Arg572Gln
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5887
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13859
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17791
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg572Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-206610547-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610547
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610547
    reference: chr 2
allele count: 3
allele frequency: 2.473777953690877e-5
allele num: 121272
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1719A>G
  hgvsp: ENST00000357785.5:c.1719A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1719A>G
  hgvsp: ENST00000272849.3:c.1719A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1719A>G
  hgvsp: ENST00000360409.3:c.1719A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1719A>G
  hgvsp: ENST00000412873.2:c.1719A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1719A>G
  hgvsp: ENST00000540841.1:c.1719A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1719A>G
  hgvsp: ENST00000540178.1:c.1719A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1719A>G
  hgvsp: ENST00000357118.4:c.1719A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2769
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6906
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17926
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17951
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Val573Val
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: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP

2-206610547-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610547
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610547
    reference: chr 2
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1719A>T
  hgvsp: ENST00000360409.3:c.1719A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1719A>T
  hgvsp: ENST00000540178.1:c.1719A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1719A>T
  hgvsp: ENST00000412873.2:c.1719A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1719A>T
  hgvsp: ENST00000272849.3:c.1719A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1719A>T
  hgvsp: ENST00000540841.1:c.1719A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1719A>T
  hgvsp: ENST00000357785.5:c.1719A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1719A>T
  hgvsp: ENST00000357118.4:c.1719A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12667
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13897
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17951
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17926
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3970
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1982
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val573Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

2-206610550-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610550
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610550
    reference: chr 2
allele count: 2
allele frequency: 1.649430121892886e-5
allele num: 121254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1722C>T
  hgvsp: ENST00000357118.4:c.1722C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1722C>T
  hgvsp: ENST00000272849.3:c.1722C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1722C>T
  hgvsp: ENST00000412873.2:c.1722C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1722C>T
  hgvsp: ENST00000540178.1:c.1722C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1722C>T
  hgvsp: ENST00000540841.1:c.1722C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1722C>T
  hgvsp: ENST00000360409.3:c.1722C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1722C>T
  hgvsp: ENST00000357785.5:c.1722C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1981
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3572
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Tyr574Tyr
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

2-206610553-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610553
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610553
    reference: chr 2
allele count: 4
allele frequency: 3.298044259753966e-5
allele num: 121284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1725G>A
  hgvsp: ENST00000540841.1:c.1725G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1725G>A
  hgvsp: ENST00000540178.1:c.1725G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1725G>A
  hgvsp: ENST00000357785.5:c.1725G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1725G>A
  hgvsp: ENST00000412873.2:c.1725G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1725G>A
  hgvsp: ENST00000272849.3:c.1725G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1725G>A
  hgvsp: ENST00000357118.4:c.1725G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1725G>A
  hgvsp: ENST00000360409.3:c.1725G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13910
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6925
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1983
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17948
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 18041
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3562
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro575Pro
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

2-206610553-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610553
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610553
    reference: chr 2
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1725G>C
  hgvsp: ENST00000412873.2:c.1725G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1725G>C
  hgvsp: ENST00000357785.5:c.1725G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1725G>C
  hgvsp: ENST00000540178.1:c.1725G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1725G>C
  hgvsp: ENST00000360409.3:c.1725G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1725G>C
  hgvsp: ENST00000272849.3:c.1725G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1725G>C
  hgvsp: ENST00000357118.4:c.1725G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1725G>C
  hgvsp: ENST00000540841.1:c.1725G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13910
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18041
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4690
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3562
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1983
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro575Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum

2-206610565-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610565
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610565
    reference: chr 2
allele count: 50
allele frequency: 4.122963256151461e-4
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1737G>A
  hgvsp: ENST00000540841.1:c.1737G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1737G>A
  hgvsp: ENST00000357785.5:c.1737G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1737G>A
  hgvsp: ENST00000272849.3:c.1737G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1737G>A
  hgvsp: ENST00000360409.3:c.1737G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1737G>A
  hgvsp: ENST00000540178.1:c.1737G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1737G>A
  hgvsp: ENST00000412873.2:c.1737G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1737G>A
  hgvsp: ENST00000357118.4:c.1737G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9928
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5890
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 13965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 6.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2766
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4694
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3976
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3559
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser579Ser
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

2-206610568-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610568
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610568
    reference: chr 2
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1740G>A
  hgvsp: ENST00000272849.3:c.1740G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1740G>A
  hgvsp: ENST00000412873.2:c.1740G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1740G>A
  hgvsp: ENST00000540841.1:c.1740G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1740G>A
  hgvsp: ENST00000360409.3:c.1740G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1740G>A
  hgvsp: ENST00000357118.4:c.1740G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1740G>A
  hgvsp: ENST00000540178.1:c.1740G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1740G>A
  hgvsp: ENST00000357785.5:c.1740G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3567
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4701
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3981
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1980
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17952
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Pro580Pro
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ

2-206610570-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610570
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610570
    reference: chr 2
allele count: 3
allele frequency: 2.473247704001715e-5
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1742C>T
  hgvsp: ENSP00000439658.1:p.Ala581Val
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1742C>T
  hgvsp: ENSP00000349632.4:p.Ala581Val
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1742C>T
  hgvsp: ENSP00000439261.1:p.Ala581Val
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1742C>T
  hgvsp: ENSP00000353582.3:p.Ala581Val
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1742C>T
  hgvsp: ENSP00000407626.2:p.Ala581Val
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1742C>T
  hgvsp: ENSP00000272849.3:p.Ala581Val
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1742C>T
  hgvsp: ENSP00000350432.5:p.Ala581Val
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12565
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5903
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17955
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala581Val
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum

2-206610571-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 206610571
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 206610571
    reference: chr 2
allele count: 34
allele frequency: 2.803060282284659e-4
allele num: 121296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000272849
  ensembl transcript: ENST00000272849
  gene symbol: NRP2
  hgvsc: ENST00000272849.3:c.1743G>A
  hgvsp: ENST00000272849.3:c.1743G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000353582
  ensembl transcript: ENST00000360409
  gene symbol: NRP2
  hgvsc: ENST00000360409.3:c.1743G>A
  hgvsp: ENST00000360409.3:c.1743G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439261
  ensembl transcript: ENST00000540841
  gene symbol: NRP2
  hgvsc: ENST00000540841.1:c.1743G>A
  hgvsp: ENST00000540841.1:c.1743G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000349632
  ensembl transcript: ENST00000357118
  gene symbol: NRP2
  hgvsc: ENST00000357118.4:c.1743G>A
  hgvsp: ENST00000357118.4:c.1743G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000350432
  ensembl transcript: ENST00000357785
  gene symbol: NRP2
  hgvsc: ENST00000357785.5:c.1743G>A
  hgvsp: ENST00000357785.5:c.1743G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000439658
  ensembl transcript: ENST00000540178
  gene symbol: NRP2
  hgvsc: ENST00000540178.1:c.1743G>A
  hgvsp: ENST00000540178.1:c.1743G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118257
  ensembl protein: ENSP00000407626
  ensembl transcript: ENST00000412873
  gene symbol: NRP2
  hgvsc: ENST00000412873.2:c.1743G>A
  hgvsp: ENST00000412873.2:c.1743G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5900
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12569
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4705
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala581Ala
num of homozygotes: 0
population: Other
population: East Asian
population: African
reference allele: G

GenotypeQuality
all individuals: 1234
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 256
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8199
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1723
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46484
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1715
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.619e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.64e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.43e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 1.696979e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.06e-1

QD
type: SiteQuality
SIO_000300: 1.436e1

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46499
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1724
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8200
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1715
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1232
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 733
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.16e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

DP
type: SiteQuality
SIO_000300: 1.697016e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.867e0

QD
type: SiteQuality
SIO_000300: 1.011e1

VQSLOD
type: SiteQuality
SIO_000300: 8.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.334e0

GenotypeQuality
all individuals: 1724
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8205
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 46511
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1714
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1231
bin: 9.75e1
variant carriers: 1

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.48e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: 8.79e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.043e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.4e0

QD
type: SiteQuality
SIO_000300: 1.371e1

DP
type: SiteQuality
SIO_000300: 1.697015e6

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46511
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1231
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1724
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1714
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 256
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8205
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 16512
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.79e-1

QD
type: SiteQuality
SIO_000300: 1.371e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.043e0

VQSLOD
type: SiteQuality
SIO_000300: 4.4e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

DP
type: SiteQuality
SIO_000300: 1.697015e6

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

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1713
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 271
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8210
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1722
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46521
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 9.75e1
variant carriers: 1

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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African
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QD
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ClippingRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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DP
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VQSLOD
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MQ
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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European (Finnish)
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East Asian
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African
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Other
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Latino
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InbreedingCoeff
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ReadPosRankSum
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DP
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MQ
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MQRankSum
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FS
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VQSLOD
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QD
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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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Other
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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FS
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DP
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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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variant carriers: 0

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

European (Non-Finnish)
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allele frequency: 1.498621268433042e-5
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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Latino
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African
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allele frequency: 0.0e0
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South Asian
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Other
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ReadPosRankSum
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MQRankSum
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FS
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InbreedingCoeff
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QD
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BaseQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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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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African
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South Asian
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allele frequency: 7.873062015503876e-4
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European (Finnish)
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European (Non-Finnish)
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Latino
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East Asian
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Other
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DP
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FS
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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MQ
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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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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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African
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Other
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Latino
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South Asian
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ReadPosRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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DP
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VQSLOD
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FS
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QD
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BaseQRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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Other
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European (Non-Finnish)
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East Asian
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South Asian
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African
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QD
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DP
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InbreedingCoeff
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MQRankSum
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FS
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MQ
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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East Asian
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European (Non-Finnish)
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European (Finnish)
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MQ
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FS
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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QD
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ReadPosRankSum
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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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bin: 5.25e1
variant carriers: 0

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

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

East Asian
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allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.835e1

MQRankSum
type: SiteQuality
SIO_000300: 1.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.59e-1

FS
type: SiteQuality
SIO_000300: 8.59e-1

VQSLOD
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SIO_000300: -2.015e0

DP
type: SiteQuality
SIO_000300: 1.693616e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.675e0

QD
type: SiteQuality
SIO_000300: 1.047e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.72e-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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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

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

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

East Asian
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allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.3e-2

InbreedingCoeff
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
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SIO_000300: -2.634e0

FS
type: SiteQuality
SIO_000300: 5.481e0

QD
type: SiteQuality
SIO_000300: 9.84e0

VQSLOD
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SIO_000300: 4.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQRankSum
type: SiteQuality
SIO_000300: 4.64e-1

DP
type: SiteQuality
SIO_000300: 1.693476e6

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 29
allele frequency: 4.346262214495534e-4
allele num: 66724
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.074410163339383e-4
allele num: 6612
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: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: -3.0e-4

BaseQRankSum
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SIO_000300: -3.479e0

DP
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SIO_000300: 1.69375e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.11e-1

MQRankSum
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SIO_000300: 2.55e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

FS
type: SiteQuality
SIO_000300: 3.244e0

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.58e-1

QD
type: SiteQuality
SIO_000300: 1.127e1

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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GenotypeQuality
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GenotypeQuality
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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: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.496268097479092e-5
allele num: 66722
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.764e0

DP
type: SiteQuality
SIO_000300: 1.691952e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e-2

FS
type: SiteQuality
SIO_000300: 2.385e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.77e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

QD
type: SiteQuality
SIO_000300: 1.102e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 908
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

ReadPosRankSum
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SIO_000300: 7.97e-1

MQRankSum
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: 3.86e0

FS
type: SiteQuality
SIO_000300: 2.905e0

DP
type: SiteQuality
SIO_000300: 1.691001e6

QD
type: SiteQuality
SIO_000300: 1.245e1

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: 3.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 3
allele frequency: 2.891844997108155e-4
allele num: 10374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.231e1

ReadPosRankSum
type: SiteQuality
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MQ
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InbreedingCoeff
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BaseQRankSum
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FS
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MQRankSum
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VQSLOD
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ClippingRankSum
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DP
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SIO_000300: 1.689186e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.349811026456296e-4
allele num: 66676
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.688544e6

ReadPosRankSum
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FS
type: SiteQuality
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BaseQRankSum
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MQRankSum
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MQ
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QD
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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SIO_000300: 1.16e0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66662
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
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 3
allele frequency: 2.896871378910776e-4
allele num: 10356
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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FS
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QD
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MQ
type: SiteQuality
SIO_000300: 5.941e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.686541e6

MQRankSum
type: SiteQuality
SIO_000300: -1.27e-1

GenotypeQuality
all individuals: 8110
bin: 6.75e1
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: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.070908207867897e-5
allele num: 16472
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.68298e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

FS
type: SiteQuality
SIO_000300: 5.365e0

VQSLOD
type: SiteQuality
SIO_000300: -1.421e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.85e-1

QD
type: SiteQuality
SIO_000300: 1.634e1

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.481086098862845e-4
allele num: 8618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
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: 908
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.149e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.71e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.43e0

FS
type: SiteQuality
SIO_000300: 1.7063e1

DP
type: SiteQuality
SIO_000300: 1.682412e6

GenotypeQuality
all individuals: 3
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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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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503578516870151e-5
allele num: 66508
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 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: 8606
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.94e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

MQRankSum
type: SiteQuality
SIO_000300: 1.84e0

VQSLOD
type: SiteQuality
SIO_000300: -1.053e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.93e-1

FS
type: SiteQuality
SIO_000300: 1.177e0

DP
type: SiteQuality
SIO_000300: 1.678336e6

QD
type: SiteQuality
SIO_000300: 1.228e1

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

GenotypeQuality
all individuals: 1593
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 237
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 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
all individuals: 45935
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variant carriers: 0

GenotypeQuality
all individuals: 1578
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506614035616356e-5
allele num: 66374
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.670369e6

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

VQSLOD
type: SiteQuality
SIO_000300: -1.883e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.41e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.43e-1

QD
type: SiteQuality
SIO_000300: 8.890000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 7594
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 592
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 45539
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1468
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GenotypeQuality
all individuals: 210
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9992
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66038
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16292
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.736676568233443e-5
allele num: 11446
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.59e-1

QD
type: SiteQuality
SIO_000300: 1.224e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e-1

FS
type: SiteQuality
SIO_000300: 6.299e0

DP
type: SiteQuality
SIO_000300: 1.647726e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.36e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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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: 6384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64818
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15936
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.210067763794773e-4
allele num: 8264
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11254
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.48e0

QD
type: SiteQuality
SIO_000300: 1.57e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.677e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.589361e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9598
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.268874508311128e-4
allele num: 15762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6312
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11144
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64128
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8172
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.555e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.131e1

VQSLOD
type: SiteQuality
SIO_000300: 2.43e-1

DP
type: SiteQuality
SIO_000300: 1.556322e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-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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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
all individuals: 736
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variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14326
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8686
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5806
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 4.048582995951417e-4
allele num: 9880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58624
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.267e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.312e1

DP
type: SiteQuality
SIO_000300: 1.275284e6

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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variant carriers: 31

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 25292
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13936
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5688
num of homozygotes: 0

African
type: Population
allele count: 26
allele frequency: 3.060263653483992e-3
allele num: 8496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7088
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.085505735140772e-4
allele num: 9590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.492107836289985e-5
allele num: 57272
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.393e1

VQSLOD
type: SiteQuality
SIO_000300: 6.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.24e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.33e-1

DP
type: SiteQuality
SIO_000300: 1.207914e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 134
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variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.054407423028258e-4
allele num: 9484
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7018
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5642
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.757654585720814e-5
allele num: 56894
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.64e-1

DP
type: SiteQuality
SIO_000300: 1.186241e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.417e0

FS
type: SiteQuality
SIO_000300: 4.312e0

QD
type: SiteQuality
SIO_000300: 1.163e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 474
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5408
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8768
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8022
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.710100231303006e-5
allele num: 12970
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53580
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.212e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.023618e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.275e0

QD
type: SiteQuality
SIO_000300: 1.152e1

GenotypeQuality
all individuals: 982
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 119
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6368
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7852
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.891414141414142e-5
allele num: 12672
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5318
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 9.74616e5

MQ
type: SiteQuality
SIO_000300: 6.011e1

QD
type: SiteQuality
SIO_000300: 8.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -8.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.71e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 222
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7752
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5116
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.424599831508003e-5
allele num: 11870
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5962
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49708
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.15e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.88e-1

DP
type: SiteQuality
SIO_000300: 8.75174e5

MQRankSum
type: SiteQuality
SIO_000300: 1.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.293e1

GenotypeQuality
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variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7750
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5970
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5120
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49676
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.450228156160216e-5
allele num: 11834
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.7e-3

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-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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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5688
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 8.49689863199932e-5
allele num: 47076
num of homozygotes: 0

Latino
type: Population
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Other
type: Population
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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
allele num: 4914
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African
type: Population
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
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BaseQRankSum
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FS
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-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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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7136
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47076
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South Asian
type: Population
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allele frequency: 1.810938065918146e-4
allele num: 11044
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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MQRankSum
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VQSLOD
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SIO_000300: 9.54e-1

FS
type: SiteQuality
SIO_000300: 3.153e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

QD
type: SiteQuality
SIO_000300: 1.25e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.94e0

DP
type: SiteQuality
SIO_000300: 8.26809e5

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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bin: 7.5e0
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 4856
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6930
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6972
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.163471939768941e-5
allele num: 46222
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

DP
type: SiteQuality
SIO_000300: 8.12619e5

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.907e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.56e0

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: 6.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42932
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.047502047502048e-4
allele num: 9768
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5122
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.764e0

DP
type: SiteQuality
SIO_000300: 7.83416e5

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.27e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16192
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517312536036173e-5
allele num: 65906
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.2e0

QD
type: SiteQuality
SIO_000300: 1.111e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.53e-1

DP
type: SiteQuality
SIO_000300: 1.969018e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.74e-1

GenotypeQuality
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bin: 8.75e1
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
all individuals: 1979
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GenotypeQuality
all individuals: 3128
bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516622179082747e-5
allele num: 65936
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6426
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.82e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.976721e6

FS
type: SiteQuality
SIO_000300: 1.828e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.232e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

QD
type: SiteQuality
SIO_000300: 9.779999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

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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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.16370808678501e-5
allele num: 16224
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66044
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.83e-1

QD
type: SiteQuality
SIO_000300: 1.313e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.0118e1

DP
type: SiteQuality
SIO_000300: 2.027124e6

VQSLOD
type: SiteQuality
SIO_000300: 5.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66126
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.748251748251748e-4
allele num: 11440
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16244
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.964e0

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

FS
type: SiteQuality
SIO_000300: 2.129e0

QD
type: SiteQuality
SIO_000300: 1.473e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

DP
type: SiteQuality
SIO_000300: 2.043346e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.35e-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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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

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

South Asian
type: Population
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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
allele num: 6456
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.512721991952319e-5
allele num: 66106
num of homozygotes: 0

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
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VQSLOD
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

ReadPosRankSum
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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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.125199068969742e-5
allele num: 16326
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6500
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66402
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
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Other
type: Population
allele count: 0
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allele num: 894
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African
type: Population
allele count: 0
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allele num: 10342
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

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

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.089e0

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 6.7e-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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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503442884204829e-5
allele num: 66514
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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: 894
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.528e0

DP
type: SiteQuality
SIO_000300: 2.102685e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.938e1

ReadPosRankSum
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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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13366
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21275
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503036132988637e-5
allele num: 66532
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.05e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.0e0

QD
type: SiteQuality
SIO_000300: 1.043e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.607e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.252999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.104293e6

GenotypeQuality
all individuals: 284
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4768
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503036132988637e-5
allele num: 66532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.607e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

DP
type: SiteQuality
SIO_000300: 2.104293e6

VQSLOD
type: SiteQuality
SIO_000300: -7.252999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.0e0

QD
type: SiteQuality
SIO_000300: 1.043e1

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66588
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

DP
type: SiteQuality
SIO_000300: 2.116461e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.149e0

VQSLOD
type: SiteQuality
SIO_000300: 4.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.659e1

GenotypeQuality
all individuals: 1227
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 1591
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3257
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.076072426783327e-5
allele num: 16458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66584
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 5.06e0

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.73e-2

DP
type: SiteQuality
SIO_000300: 2.723722e6

FS
type: SiteQuality
SIO_000300: 5.31e-1

QD
type: SiteQuality
SIO_000300: 1.499e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.732e0

GenotypeQuality
all individuals: 1227
bin: 8.75e1
variant carriers: 62

GenotypeQuality
all individuals: 123
bin: 4.25e1
variant carriers: 25

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 4

GenotypeQuality
all individuals: 176
bin: 3.75e1
variant carriers: 19

GenotypeQuality
all individuals: 3257
bin: 7.75e1
variant carriers: 69

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 8

GenotypeQuality
all individuals: 236
bin: 5.25e1
variant carriers: 35

GenotypeQuality
all individuals: 200
bin: 3.25e1
variant carriers: 16

GenotypeQuality
all individuals: 171
bin: 5.75e1
variant carriers: 28

GenotypeQuality
all individuals: 28004
bin: 9.75e1
variant carriers: 19311

GenotypeQuality
all individuals: 1591
bin: 9.25e1
variant carriers: 103

South Asian
type: Population
allele count: 3786
allele frequency: 2.300401020780168e-1
allele num: 16458
num of homozygotes: 475

African
type: Population
allele count: 2002
allele frequency: 1.929824561403509e-1
allele num: 10374
num of homozygotes: 182

European (Finnish)
type: Population
allele count: 819
allele frequency: 1.250763591936469e-1
allele num: 6548
num of homozygotes: 45

European (Non-Finnish)
type: Population
allele count: 9008
allele frequency: 1.352877568184549e-1
allele num: 66584
num of homozygotes: 605

Latino
type: Population
allele count: 2878
allele frequency: 2.500868960722976e-1
allele num: 11508
num of homozygotes: 350

East Asian
type: Population
allele count: 3861
allele frequency: 4.480157809236482e-1
allele num: 8618
num of homozygotes: 866

Other
type: Population
allele count: 166
allele frequency: 1.852678571428572e-1
allele num: 896
num of homozygotes: 16

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.73e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.06e0

DP
type: SiteQuality
SIO_000300: 2.723722e6

FS
type: SiteQuality
SIO_000300: 5.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.732e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 1.499e1

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 245
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GenotypeQuality
all individuals: 2765
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variant carriers: 0

GenotypeQuality
all individuals: 17946
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 128
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 17516
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 188
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variant carriers: 0

GenotypeQuality
all individuals: 6802
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500915558490679e-5
allele num: 66626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.33993e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.005e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

VQSLOD
type: SiteQuality
SIO_000300: 3.99e0

MQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

QD
type: SiteQuality
SIO_000300: 1.058e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

GenotypeQuality
all individuals: 97
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1975
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 169
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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: 4662
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variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5004651441947e-5
allele num: 66646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.94e-1

DP
type: SiteQuality
SIO_000300: 2.34061e6

MQ
type: SiteQuality
SIO_000300: 5.885e1

MQRankSum
type: SiteQuality
SIO_000300: 4.43e-1

FS
type: SiteQuality
SIO_000300: 2.001e0

VQSLOD
type: SiteQuality
SIO_000300: -3.169e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 8.220000000000001e0

GenotypeQuality
all individuals: 162
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1978
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
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GenotypeQuality
all individuals: 3565
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GenotypeQuality
all individuals: 240
bin: 2.25e1
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GenotypeQuality
all individuals: 3954
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variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2762
bin: 9.25e1
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GenotypeQuality
all individuals: 165
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6841
bin: 6.75e1
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GenotypeQuality
all individuals: 17847
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.50112528132033e-5
allele num: 66650
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.272e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

FS
type: SiteQuality
SIO_000300: 2.353e0

VQSLOD
type: SiteQuality
SIO_000300: 6.840000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.341317e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.564e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.144e1

GenotypeQuality
all individuals: 138
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4664
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GenotypeQuality
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GenotypeQuality
all individuals: 1980
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 197
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GenotypeQuality
all individuals: 3961
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.628345850182938e-5
allele num: 10386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66662
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.69e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.119e0

FS
type: SiteQuality
SIO_000300: 5.69e-1

DP
type: SiteQuality
SIO_000300: 2.342394e6

QD
type: SiteQuality
SIO_000300: 1.563e1

VQSLOD
type: SiteQuality
SIO_000300: -9.87e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e0

GenotypeQuality
all individuals: 17949
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2767
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GenotypeQuality
all individuals: 1979
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variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 5.25e1
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GenotypeQuality
all individuals: 3956
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variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3581
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GenotypeQuality
all individuals: 6875
bin: 6.75e1
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GenotypeQuality
all individuals: 4686
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GenotypeQuality
all individuals: 140
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
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South Asian
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African
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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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European (Non-Finnish)
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allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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DP
type: SiteQuality
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VQSLOD
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MQ
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QD
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ClippingRankSum
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FS
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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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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Latino
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allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
allele num: 10390
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European (Non-Finnish)
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allele frequency: 1.499835018148004e-5
allele num: 66674
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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InbreedingCoeff
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ReadPosRankSum
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FS
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MQRankSum
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DP
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MQ
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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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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African
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allele frequency: 9.626492106276473e-5
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

Other
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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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South Asian
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DP
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ClippingRankSum
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FS
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InbreedingCoeff
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MQ
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQRankSum
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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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Latino
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allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

East Asian
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num of homozygotes: 0

South Asian
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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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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.5346e1

MQRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 5.953e1

QD
type: SiteQuality
SIO_000300: 1.671e1

VQSLOD
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SIO_000300: -7.654e-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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Other
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allele num: 898
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

East Asian
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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

African
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allele frequency: 0.0e0
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Latino
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ClippingRankSum
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ReadPosRankSum
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FS
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DP
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQRankSum
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.941e1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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Other
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

VQSLOD
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MQRankSum
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ReadPosRankSum
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QD
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MQ
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ClippingRankSum
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InbreedingCoeff
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DP
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FS
type: SiteQuality
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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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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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European (Non-Finnish)
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allele num: 66662
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African
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European (Finnish)
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Other
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East Asian
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FS
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MQ
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InbreedingCoeff
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QD
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VQSLOD
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MQRankSum
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DP
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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European (Finnish)
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Latino
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East Asian
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South Asian
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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FS
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MQ
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66698
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European (Finnish)
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East Asian
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South Asian
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African
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Latino
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DP
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InbreedingCoeff
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QD
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ClippingRankSum
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FS
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MQ
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BaseQRankSum
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MQRankSum
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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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African
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Latino
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Other
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South Asian
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QD
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FS
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MQ
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -7.52e-1

DP
type: SiteQuality
SIO_000300: 2.347906e6

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.97e-1

GenotypeQuality
all individuals: 2771
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4690
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3978
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 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: 4
allele frequency: 5.996641880546894e-5
allele num: 66704
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.75e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.13e-1

FS
type: SiteQuality
SIO_000300: 4.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.57e0

DP
type: SiteQuality
SIO_000300: 2.348487e6

MQ
type: SiteQuality
SIO_000300: 5.941e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.91e-1

QD
type: SiteQuality
SIO_000300: 1.317e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.066e0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6925
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17948
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 183
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2771
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3978
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.066e0

MQRankSum
type: SiteQuality
SIO_000300: -6.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.941e1

FS
type: SiteQuality
SIO_000300: 4.37e-1

QD
type: SiteQuality
SIO_000300: 1.317e1

DP
type: SiteQuality
SIO_000300: 2.348487e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.91e-1

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17801
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 153
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1978
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17978
bin: 9.75e1
variant carriers: 50

GenotypeQuality
all individuals: 6896
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.184929139301763e-4
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 43
allele frequency: 4.136206233166602e-3
allele num: 10396
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

DP
type: SiteQuality
SIO_000300: 2.350647e6

MQRankSum
type: SiteQuality
SIO_000300: 3.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.72e-1

QD
type: SiteQuality
SIO_000300: 1.405e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.6e0

GenotypeQuality
all individuals: 17924
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2767
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 98
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6923
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 125
bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.769e0

MQRankSum
type: SiteQuality
SIO_000300: 2.43e-1

FS
type: SiteQuality
SIO_000300: 2.722e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

DP
type: SiteQuality
SIO_000300: 2.349427e6

QD
type: SiteQuality
SIO_000300: 8.779999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

GenotypeQuality
all individuals: 3981
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6950
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18132
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2768
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3567
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4711
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1980
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49802087081684e-5
allele num: 66696
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.921e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.85e-1

FS
type: SiteQuality
SIO_000300: 2.479e0

DP
type: SiteQuality
SIO_000300: 2.350756e6

QD
type: SiteQuality
SIO_000300: 8.92e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.995e0

GenotypeQuality
all individuals: 82
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3981
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3567
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6957
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17973
bin: 9.75e1
variant carriers: 34

GenotypeQuality
all individuals: 2770
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18156
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1976
bin: 8.75e1
variant carriers: 0

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

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

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