18-55862942-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55862942
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55862942
    reference: chr 18
allele count: 25
allele frequency: 2.228958630527817e-4
allele num: 112160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29849C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29849C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29849C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-343C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29849C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29849C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29849C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151002C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-265C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29849C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29849C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29849C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29849C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29849C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29849C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29849C>T
  variant of: http://identifiers.org/hgnc/7728
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14966
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 32476
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-55862946-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55862946
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55862946
    reference: chr 18
allele count: 1
allele frequency: 8.913768206371561e-6
allele num: 112186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29853C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-261C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29853C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29853C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29853C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-339C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29853C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29853C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29853C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29853C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29853C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29853C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29853C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29853C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151006C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29853C>T
  variant of: http://identifiers.org/hgnc/7728
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15021
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/18-55862951-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55862951
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55862951
    reference: chr 18
allele count: 1
allele frequency: 8.90805109658109e-6
allele num: 112258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-256C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29858C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29858C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29858C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-334C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29858C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29858C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29858C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29858C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151011C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29858C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29858C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29858C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29858C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29858C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29858C>A
  variant of: http://identifiers.org/hgnc/7728
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32430
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

18-55862957-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55862957
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55862957
    reference: chr 18
allele count: 3
allele frequency: 2.671939293539251e-5
allele num: 112278
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29864T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29864T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29864T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29864T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29864T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29864T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29864T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151017T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29864T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29864T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-328T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29864T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-250T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29864T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29864T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29864T>G
  variant of: http://identifiers.org/hgnc/7728
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

18-55862961-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55862961
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55862961
    reference: chr 18
allele count: 1
allele frequency: 8.904719501335708e-6
allele num: 112300
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29868A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29868A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29868A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29868A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29868A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29868A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29868A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29868A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29868A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29868A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-324A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-246A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29868A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29868A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29868A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151021A>G
  variant of: http://identifiers.org/hgnc/7728
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

18-55862966-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55862966
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55862966
    reference: chr 18
allele count: 3
allele frequency: 2.671986889450996e-5
allele num: 112276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29873G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151026G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29873G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-320+1G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-242+1G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29873G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29873G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29873G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29873G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29873G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29873G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29873G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29873G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29873G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29873G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29873G>A
  variant of: http://identifiers.org/hgnc/7728
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.-242+1G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

18-55862971-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55862971
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55862971
    reference: chr 18
allele count: 93
allele frequency: 8.284044751656809e-4
allele num: 112264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29878T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29878T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29878T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29878T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29878T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29878T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29878T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151031T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29878T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-242+6T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29878T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-320+6T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29878T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29878T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29878T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29878T>C
  variant of: http://identifiers.org/hgnc/7728
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31715
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.-242+6T>C
num of homozygotes: 2
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ

18-55862972-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55862972
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55862972
    reference: chr 18
allele count: 1
allele frequency: 8.909003438875328e-6
allele num: 112246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151032G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29879G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29879G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29879G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-242+7G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29879G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29879G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29879G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29879G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-320+7G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29879G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29879G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29879G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29879G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29879G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29879G>A
  variant of: http://identifiers.org/hgnc/7728
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.-242+7G>A
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/18-55862977-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55862977
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55862977
    reference: chr 18
allele count: 1
allele frequency: 8.912814845184407e-6
allele num: 112198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29884C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29884C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29884C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29884C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29884C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29884C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29884C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-320+12C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29884C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29884C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29884C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-242+12C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29884C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29884C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29884C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151037C>A
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15233
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

18-55862977-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55862977
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55862977
    reference: chr 18
allele count: 2
allele frequency: 1.782562969036881e-5
allele num: 112198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-320+12C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29884C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151037C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29884C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29884C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29884C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29884C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29884C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-242+12C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29884C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29884C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29884C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29884C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29884C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29884C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29884C>T
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

18-55862978-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55862978
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55862978
    reference: chr 18
allele count: 330
allele frequency: 2.940652290144359e-3
allele num: 112220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29885G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29885G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29885G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29885G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29885G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-320+13G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29885G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29885G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29885G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-242+13G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29885G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29885G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29885G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151038G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29885G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29885G>A
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 3.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 31128
  bin: 2.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
num of homozygotes: 1
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

18-55862981-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55862981
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55862981
    reference: chr 18
allele count: 1
allele frequency: 8.910908734472741e-6
allele num: 112222
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29888G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29888G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29888G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29888G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-242+16G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29888G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29888G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29888G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29888G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29888G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29888G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29888G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151041G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-320+16G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29888G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29888G>C
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

18-55862986-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55862986
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55862986
    reference: chr 18
allele count: 2
allele frequency: 1.782626521917393e-5
allele num: 112194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29893C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29893C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151046C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29893C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29893C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29893C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-242+21C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29893C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29893C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-320+21C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29893C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29893C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29893C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29893C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29893C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29893C>T
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14931
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

18-55862987-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55862987
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55862987
    reference: chr 18
allele count: 1
allele frequency: 8.914562829838824e-6
allele num: 112176
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29894G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29894G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29894G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29894G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29894G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29894G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29894G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29894G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151047G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29894G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29894G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-320+22G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29894G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-242+22G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29894G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29894G>A
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5542
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

18-55862987-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55862987
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55862987
    reference: chr 18
allele count: 1
allele frequency: 8.914562829838824e-6
allele num: 112176
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29894G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29894G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29894G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29894G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29894G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29894G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29894G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29894G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29894G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-242+22G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-320+22G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29894G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29894G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151047G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29894G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29894G>C
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5542
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14886
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS

18-55862996-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55862996
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55862996
    reference: chr 18
allele count: 2
allele frequency: 1.78345312193469e-5
allele num: 112142
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29903A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29903A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29903A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-320+31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29903A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29903A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29903A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29903A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29903A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151056A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29903A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29903A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29903A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-242+31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29903A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29903A>G
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5269
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/18-55863002-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55863002
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55863002
    reference: chr 18
allele count: 2
allele frequency: 1.785937527905274e-5
allele num: 111986
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29909C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-242+37C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29909C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151062C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29909C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29909C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-320+37C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29909C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29909C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29909C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29909C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29909C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29909C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29909C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29909C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29909C>A
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

18-55863002-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55863002
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55863002
    reference: chr 18
allele count: 1
allele frequency: 8.92968763952637e-6
allele num: 111986
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29909C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29909C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29909C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29909C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29909C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29909C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29909C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151062C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29909C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-242+37C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29909C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29909C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-320+37C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29909C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29909C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29909C>T
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4826
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP

18-55863003-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55863003
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55863003
    reference: chr 18
allele count: 1
allele frequency: 8.926021136818052e-6
allele num: 112032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29910G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29910G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29910G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29910G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29910G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29910G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29910G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-320+38G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29910G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151063G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-242+38G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29910G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29910G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29910G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29910G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29910G>A
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum

18-55863006-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55863006
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55863006
    reference: chr 18
allele count: 72
allele frequency: 6.42535874919683e-4
allele num: 112056
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29913T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29913T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29913T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29913T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29913T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29913T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29913T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151066T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29913T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29913T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29913T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29913T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-320+41T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29913T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-242+41T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29913T>C
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13100
  bin: 2.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

18-55863007-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55863007
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55863007
    reference: chr 18
allele count: 1
allele frequency: 8.926180487369454e-6
allele num: 112030
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.159+29914A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.98+29914A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-320+29914A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.122+29914A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.122+29914A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.170+29914A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.98+29914A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-301+29914A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-242+42A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.122+29914A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1222+29914A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-320+42A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-242+29914A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-242+29914A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.48+151067A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.122+29914A>G
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5161
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

18-55912631-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912631
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912631
    reference: chr 18
allele count: 2
allele frequency: 8.538251366120219e-5
allele num: 23424
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-241-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-241-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-241-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.187-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-241-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.123-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-190-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.102-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-241-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.123-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-145247C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-241-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1223-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.171-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.160-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.99-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.123-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.99-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-241-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-241-28C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.123-28C>T
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

18-55912656-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912656
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912656
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 27404
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.123-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-241-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-241-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.123-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.171-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-241-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-190-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.187-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.99-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.102-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.160-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.99-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-241-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.123-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-241-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.123-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-145222C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1223-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-241-3C>T
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.123-3C>T
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

18-55912665-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912665
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912665
    reference: chr 18
allele count: 2
allele frequency: 6.399590426212723e-5
allele num: 31252
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.129G>A
  hgvsp: ENST00000382850.4:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-235G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.105G>A
  hgvsp: ENST00000357895.5:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.108G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.129G>A
  hgvsp: ENST00000356462.6:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1229G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-235G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-235G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.129G>A
  hgvsp: ENST00000256830.9:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.193G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-235G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-235G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-235G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-235G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.129G>A
  hgvsp: ENST00000400345.3:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-235G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.166G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-145213G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-184G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.105G>A
  hgvsp: ENST00000586263.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro43Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

18-55912665-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912665
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912665
    reference: chr 18
allele count: 4
allele frequency: 1.279918085242545e-4
allele num: 31252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.129G>T
  hgvsp: ENST00000382850.4:c.129G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-235G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.105G>T
  hgvsp: ENST00000586263.1:c.105G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.129G>T
  hgvsp: ENST00000256830.9:c.129G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-235G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.129G>T
  hgvsp: ENST00000400345.3:c.129G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.129G>T
  hgvsp: ENST00000356462.6:c.129G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-235G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.193G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-145213G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-235G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.105G>T
  hgvsp: ENST00000357895.5:c.105G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.177G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1229G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.108G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-235G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-184G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-235G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-235G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-235G>T
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro43Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

18-55912669-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912669
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912669
    reference: chr 18
allele count: 1
allele frequency: 3.019688368160406e-5
allele num: 33116
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-231G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1233G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.133G>C
  hgvsp: ENSP00000372301.3:p.Val45Leu
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.109G>C
  hgvsp: ENSP00000468546.1:p.Val37Leu
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-231G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.170G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.133G>C
  hgvsp: ENSP00000348847.5:p.Val45Leu
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.109G>C
  hgvsp: ENSP00000350569.4:p.Val37Leu
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-231G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-231G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-231G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.181G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.112G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.133G>C
  hgvsp: ENSP00000256830.8:p.Val45Leu
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.133G>C
  hgvsp: ENSP00000383199.2:p.Val45Leu
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-231G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-231G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-180G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-231G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-145209G>C
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val45Leu
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

18-55912675-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912675
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912675
    reference: chr 18
allele count: 1
allele frequency: 2.770543580650524e-5
allele num: 36094
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.139C>T
  hgvsp: ENSP00000256830.8:p.Leu47Phe
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-225C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-225C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-225C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.115C>T
  hgvsp: ENSP00000468546.1:p.Leu39Phe
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-145203C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.176C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.203C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.139C>T
  hgvsp: ENSP00000372301.3:p.Leu47Phe
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-225C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1239C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.139C>T
  hgvsp: ENSP00000348847.5:p.Leu47Phe
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.187C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.118C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.115C>T
  hgvsp: ENSP00000350569.4:p.Leu39Phe
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-225C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-225C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-174C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-225C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-225C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.139C>T
  hgvsp: ENSP00000383199.2:p.Leu47Phe
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu47Phe
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

18-55912686-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912686
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912686
    reference: chr 18
allele count: 2
allele frequency: 4.911591355599214e-5
allele num: 40720
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.126C>T
  hgvsp: ENST00000357895.5:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-214C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-145192C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.129C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-214C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.187C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.150C>T
  hgvsp: ENST00000400345.3:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.126C>T
  hgvsp: ENST00000586263.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-214C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-214C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1250C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-214C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.150C>T
  hgvsp: ENST00000382850.4:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-163C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.150C>T
  hgvsp: ENST00000356462.6:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.150C>T
  hgvsp: ENST00000256830.9:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.198C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-214C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.214C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-214C>T
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Tyr50Tyr
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

18-55912692-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912692
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912692
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 43308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.132G>A
  hgvsp: ENST00000357895.5:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-208G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-208G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-208G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-208G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-157G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-208G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.156G>A
  hgvsp: ENST00000382850.4:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.135G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.156G>A
  hgvsp: ENST00000400345.3:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.132G>A
  hgvsp: ENST00000586263.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-208G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.204G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.156G>A
  hgvsp: ENST00000356462.6:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.156G>A
  hgvsp: ENST00000256830.9:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-208G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.193G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1256G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-145186G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-208G>A
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala52Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

18-55912696-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912696
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912696
    reference: chr 18
allele count: 1
allele frequency: 2.24870699347875e-5
allele num: 44470
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-153G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.160G>A
  hgvsp: ENSP00000348847.5:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-204G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.197G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-204G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.136G>A
  hgvsp: ENSP00000468546.1:p.Glu46Lys
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-204G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-204G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-204G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.136G>A
  hgvsp: ENSP00000350569.4:p.Glu46Lys
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.160G>A
  hgvsp: ENSP00000372301.3:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.160G>A
  hgvsp: ENSP00000256830.8:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.208G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.224G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.160G>A
  hgvsp: ENSP00000383199.2:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-204G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-204G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-145182G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1260G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-204G>A
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu54Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

18-55912699-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912699
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912699
    reference: chr 18
allele count: 14
allele frequency: 3.090507726269316e-4
allele num: 45300
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-201A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-201A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.139A>G
  hgvsp: ENSP00000468546.1:p.Asn47Asp
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-201A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.163A>G
  hgvsp: ENSP00000256830.8:p.Asn55Asp
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.227A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.163A>G
  hgvsp: ENSP00000348847.5:p.Asn55Asp
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-201A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-201A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-201A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.163A>G
  hgvsp: ENSP00000372301.3:p.Asn55Asp
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.163A>G
  hgvsp: ENSP00000383199.2:p.Asn55Asp
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-150A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-201A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000591989
  gene symbol: NEDD4L
  hgvsc: ENST00000591989.1:n.211A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1263A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.139A>G
  hgvsp: ENSP00000350569.4:p.Asn47Asp
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-201A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.200A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-145179A>G
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn55Asp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

18-55912730-CAATTA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912730
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912725
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 42274
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-167_-163delTTAAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.197_201delTTAAA
  hgvsp: ENSP00000383199.2:p.Ile66LysfsTer9
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.173_177delTTAAA
  hgvsp: ENSP00000350569.4:p.Ile58LysfsTer9
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-167_-163delTTAAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.261_265delTTAAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-167_-163delTTAAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.197_201delTTAAA
  hgvsp: ENSP00000348847.5:p.Ile66LysfsTer9
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.197_201delTTAAA
  hgvsp: ENSP00000372301.3:p.Ile66LysfsTer9
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-167_-163delTTAAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.173_177delTTAAA
  hgvsp: ENSP00000468546.1:p.Ile58LysfsTer9
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-167_-163delTTAAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1296_1300delATTAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-167_-163delTTAAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-167_-163delTTAAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.197_201delTTAAA
  hgvsp: ENSP00000256830.8:p.Ile66LysfsTer9
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-167_-163delTTAAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-116_-112delTTAAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.233_237delATTAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.176_180delTTAAA
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: frameshift
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile66LysfsTer9
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: CAATTA
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

18-55912733-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912733
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912733
    reference: chr 18
allele count: 1
allele frequency: 2.401421641611834e-5
allele num: 41642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-167T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-167T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.173T>A
  hgvsp: ENSP00000350569.4:p.Ile58Asn
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.173T>A
  hgvsp: ENSP00000468546.1:p.Ile58Asn
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-116T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-167T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.176T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.197T>A
  hgvsp: ENSP00000372301.3:p.Ile66Asn
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.197T>A
  hgvsp: ENSP00000256830.8:p.Ile66Asn
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588516
  gene symbol: NEDD4L
  hgvsc: ENST00000588516.1:n.1297T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-167T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.197T>A
  hgvsp: ENSP00000383199.2:p.Ile66Asn
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.197T>A
  hgvsp: ENSP00000348847.5:p.Ile66Asn
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-145145T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585363
  gene symbol: NEDD4L
  hgvsc: ENST00000585363.1:n.234T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-167T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-167T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-167T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-167T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.261T>A
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile66Asn
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

18-55912745-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912745
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912745
    reference: chr 18
allele count: 1
allele frequency: 2.542717656631408e-5
allele num: 39328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-160+5G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-109+5G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.204+5G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-160+5G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-160+5G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-160+5G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.183+5G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-160+5G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.180+5G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-160+5G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-145133G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.268+5G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.204+5G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-160+5G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-160+5G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.180+5G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.204+5G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.204+5G>C
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.204+5G>C
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

18-55912749-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912749
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912749
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 37646
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.204+9C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-160+9C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-109+9C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.183+9C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.204+9C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-160+9C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.204+9C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-160+9C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-160+9C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-160+9C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.268+9C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.180+9C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-160+9C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.204+9C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-160+9C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-145129C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.180+9C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-160+9C>T
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ

18-55912752-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912752
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912752
    reference: chr 18
allele count: 1
allele frequency: 2.678810608090008e-5
allele num: 37330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-160+12T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-160+12T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-109+12T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-160+12T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.204+12T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.180+12T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.180+12T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.204+12T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-160+12T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.204+12T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.268+12T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-160+12T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-160+12T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.183+12T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.204+12T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-160+12T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-160+12T>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-145126T>A
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24545
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16405
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

18-55912768-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912768
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912768
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 30130
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-160+28A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-145110A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.204+28A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-160+28A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-160+28A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-109+28A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.204+28A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.204+28A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.268+28A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.180+28A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-160+28A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-160+28A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.180+28A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-160+28A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-160+28A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-160+28A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.183+28A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.204+28A>G
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5643
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19701
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23841
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

18-55912769-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912769
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912769
    reference: chr 18
allele count: 2
allele frequency: 6.634819532908705e-5
allele num: 30144
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-160+29T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-145109T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.204+29T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.180+29T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-109+29T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-160+29T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-160+29T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.180+29T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.183+29T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-160+29T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.204+29T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-160+29T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-160+29T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.204+29T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.268+29T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-160+29T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.204+29T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-160+29T>C
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5628
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD

18-55912771-TAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55912771
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55912769
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 29214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-145106_49-145105delAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.183+32_183+33delAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.204+32_204+33delAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-160+32_-160+33delAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.204+32_204+33delAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-160+32_-160+33delAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.268+32_268+33delAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-160+32_-160+33delAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.180+32_180+33delAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-160+32_-160+33delAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-160+32_-160+33delAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.204+32_204+33delAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-160+32_-160+33delAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.204+32_204+33delAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-109+32_-109+33delAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-160+32_-160+33delAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-160+32_-160+33delAA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.180+32_180+33delAA
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: TAA
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/18-55916093-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55916093
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55916093
    reference: chr 18
allele count: 1
allele frequency: 4.471472008585226e-5
allele num: 22364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-159-38A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-159-38A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.205-38A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-159-38A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.205-38A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.181-38A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-141785A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.205-38A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-159-38A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.345-38A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-159-38A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.181-38A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-108-38A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-159-38A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-159-38A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.269-38A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-159-38A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.205-38A>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.184-38A>C
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

18-55916100-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55916100
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55916100
    reference: chr 18
allele count: 1
allele frequency: 4.47267197423741e-5
allele num: 22358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.205-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-159-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-108-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-159-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-159-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-159-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-159-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-159-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.181-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-159-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.205-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.205-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.181-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.184-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.345-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.269-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.205-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-159-31A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-141778A>G
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-55916107-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55916107
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55916107
    reference: chr 18
allele count: 2
allele frequency: 8.940545373267769e-5
allele num: 22370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-141771A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-159-24A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.181-24A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.205-24A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.205-24A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-159-24A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-159-24A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.184-24A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-159-24A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.205-24A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.345-24A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.269-24A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.181-24A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-159-24A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-159-24A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-159-24A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-108-24A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.205-24A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-159-24A>G
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

18-55916114-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55916114
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55916114
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 22404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-159-17G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.205-17G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.205-17G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.181-17G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-159-17G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-159-17G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-159-17G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.184-17G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.181-17G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-159-17G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.205-17G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-159-17G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-141764G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-159-17G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.205-17G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.345-17G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-108-17G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-159-17G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.269-17G>T
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ

18-55916115-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55916115
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55916115
    reference: chr 18
allele count: 1
allele frequency: 4.461099214846538e-5
allele num: 22416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.205-16A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-108-16A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-159-16A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.269-16A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-159-16A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.184-16A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-159-16A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-159-16A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-159-16A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-141763A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.205-16A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-159-16A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-159-16A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.205-16A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.181-16A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.205-16A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-159-16A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.345-16A>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.181-16A>T
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

18-55916128-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55916128
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55916128
    reference: chr 18
allele count: 1
allele frequency: 4.455930843953302e-5
allele num: 22442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-159-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.269-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.181-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-159-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-159-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-159-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-159-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.181-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.184-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-159-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.205-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-159-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.205-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.205-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.345-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.205-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-159-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-108-3C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-141750C>T
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.205-3C>T
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

18-55916132-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55916132
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55916132
    reference: chr 18
allele count: 1
allele frequency: 4.45751983596327e-5
allele num: 22434
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.206C>T
  hgvsp: ENSP00000348847.5:p.Thr69Ile
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-141746C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.346C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.206C>T
  hgvsp: ENSP00000256830.8:p.Thr69Ile
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-158C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.185C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-158C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-158C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.206C>T
  hgvsp: ENSP00000383199.2:p.Thr69Ile
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.182C>T
  hgvsp: ENSP00000468546.1:p.Thr61Ile
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-158C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-107C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.270C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.182C>T
  hgvsp: ENSP00000350569.4:p.Thr61Ile
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.206C>T
  hgvsp: ENSP00000372301.3:p.Thr69Ile
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-158C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-158C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-158C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-158C>T
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr69Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

18-55916136-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55916136
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55916136
    reference: chr 18
allele count: 1
allele frequency: 4.453946196329948e-5
allele num: 22452
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.210G>C
  hgvsp: ENST00000356462.6:c.210G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-154G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.186G>C
  hgvsp: ENST00000586263.1:c.186G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.189G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-154G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-154G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-154G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.210G>C
  hgvsp: ENST00000256830.9:c.210G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.210G>C
  hgvsp: ENST00000382850.4:c.210G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-154G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-103G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-141742G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.186G>C
  hgvsp: ENST00000357895.5:c.186G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.210G>C
  hgvsp: ENST00000400345.3:c.210G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-154G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-154G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.274G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.350G>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-154G>C
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu70Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

18-55916181-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55916181
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55916181
    reference: chr 18
allele count: 1
allele frequency: 4.818812644564379e-5
allele num: 20752
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.243+12A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-121+12A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-121+12A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-121+12A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.222+12A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-141697A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-121+12A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.243+12A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.243+12A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-121+12A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-121+12A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.219+12A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.219+12A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-121+12A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.383+12A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.307+12A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-121+12A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.243+12A>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-70+12A>G
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29717
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

18-55916192-ATAAT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55916192
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55916188
    reference: chr 18
allele count: 3
allele frequency: 1.478560867422376e-4
allele num: 20290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.222+25_222+28delAATT
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-121+25_-121+28delAATT
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-121+25_-121+28delAATT
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-121+25_-121+28delAATT
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.383+25_383+28delAATT
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.243+25_243+28delAATT
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.219+25_219+28delAATT
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-121+25_-121+28delAATT
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-121+25_-121+28delAATT
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.243+25_243+28delAATT
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.243+25_243+28delAATT
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-121+25_-121+28delAATT
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-121+25_-121+28delAATT
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.307+25_307+28delAATT
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.219+25_219+28delAATT
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-70+25_-70+28delAATT
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.243+25_243+28delAATT
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-121+25_-121+28delAATT
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: ATAAT
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD

18-55916196-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55916196
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55916196
    reference: chr 18
allele count: 1
allele frequency: 4.965736418710895e-5
allele num: 20138
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-121+27T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.219+27T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.243+27T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.307+27T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-121+27T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.243+27T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.219+27T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.383+27T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-141682T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-121+27T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-121+27T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-121+27T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.243+27T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-121+27T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.222+27T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.243+27T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-121+27T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-70+27T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-121+27T>C
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

18-55916202-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55916202
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55916202
    reference: chr 18
allele count: 1
allele frequency: 5.044390637610976e-5
allele num: 19824
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.243+33T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.243+33T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-121+33T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-70+33T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-121+33T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.222+33T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-121+33T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-121+33T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-141676T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.383+33T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-121+33T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.243+33T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.219+33T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.243+33T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.219+33T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.307+33T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-121+33T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-121+33T>C
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-121+33T>C
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

18-55916208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55916208
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55916208
    reference: chr 18
allele count: 2
allele frequency: 1.047888504663104e-4
allele num: 19086
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-121+39C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-141670C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-121+39C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.222+39C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.383+39C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.219+39C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-121+39C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.243+39C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.243+39C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.219+39C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-121+39C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.307+39C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-121+39C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-121+39C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-121+39C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.243+39C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.243+39C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-70+39C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-121+39C>T
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

18-55916218-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55916218
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55916218
    reference: chr 18
allele count: 1
allele frequency: 5.410084397316598e-5
allele num: 18484
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.307+49G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.383+49G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-121+49G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.243+49G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-121+49G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.243+49G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.243+49G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.243+49G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.219+49G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-121+49G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-121+49G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-121+49G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-121+49G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-121+49G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-141660G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.222+49G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-121+49G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.219+49G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-70+49G>A
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

18-55919191-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55919191
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55919191
    reference: chr 18
allele count: 486
allele frequency: 4.116690384224436e-3
allele num: 118056
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-120-42G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-120-42G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.308-42G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-120-42G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-138687G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.384-42G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.244-42G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-120-42G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-120-42G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-120-42G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.220-42G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.220-42G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.244-42G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-120-42G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.223-42G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.244-42G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-69-42G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-120-42G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.244-42G>A
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14512
  bin: 2.25e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5503
  bin: 1.75e1
  variant carriers: 58
genotype quality: GenotypeQuality
num of homozygotes: 3
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

18-55919199-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55919199
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55919199
    reference: chr 18
allele count: 49
allele frequency: 4.142572114571709e-4
allele num: 118284
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.244-34C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.220-34C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-120-34C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.244-34C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-138679C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-120-34C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-120-34C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.384-34C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-120-34C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.308-34C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-120-34C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-120-34C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-120-34C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-120-34C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.223-34C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.244-34C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.244-34C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-69-34C>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.220-34C>T
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

18-55919202-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55919202
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55919202
    reference: chr 18
allele count: 16
allele frequency: 1.35139700665563e-4
allele num: 118396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.244-31G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.308-31G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.220-31G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-138676G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.220-31G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.244-31G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-69-31G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-120-31G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-120-31G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.223-31G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-120-31G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.244-31G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.384-31G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-120-31G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-120-31G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-120-31G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-120-31G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.244-31G>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-120-31G>A
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7136
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

18-55919202-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55919202
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55919202
    reference: chr 18
allele count: 3
allele frequency: 2.533869387479307e-5
allele num: 118396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.244-31G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-120-31G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-69-31G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.220-31G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.223-31G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-120-31G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.244-31G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.308-31G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-120-31G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-120-31G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-120-31G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.384-31G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-120-31G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.244-31G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-138676G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-120-31G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.220-31G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.244-31G>T
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-120-31G>T
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ

18-55919205-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55919205
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55919204
    reference: chr 18
allele count: 12
allele frequency: 1.011975037949064e-4
allele num: 118580
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.223-22delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-120-22delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.244-22delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-120-22delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-120-22delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.308-22delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.220-22delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-69-22delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-120-22delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-138667delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.244-22delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-120-22delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.384-22delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.220-22delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-120-22delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-120-22delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.244-22delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-120-22delA
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.244-22delA
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
reference allele: TA
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

18-55919214-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55919214
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55919214
    reference: chr 18
allele count: 1
allele frequency: 8.396587626788473e-6
allele num: 119096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.220-19C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.384-19C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-120-19C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.244-19C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.223-19C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.308-19C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-120-19C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-120-19C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-120-19C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-120-19C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-138664C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-120-19C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.244-19C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.244-19C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-69-19C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-120-19C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.244-19C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.220-19C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-120-19C>G
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

18-55919225-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55919225
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55919225
    reference: chr 18
allele count: 1
allele frequency: 8.356592515835743e-6
allele num: 119666
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-138653C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-120-8C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-120-8C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.308-8C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.244-8C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.244-8C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-120-8C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-69-8C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.220-8C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.244-8C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-120-8C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.244-8C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.220-8C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-120-8C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-120-8C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.384-8C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-120-8C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.223-8C>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-120-8C>G
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.244-8C>G
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/18-55919226-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55919226
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55919226
    reference: chr 18
allele count: 1
allele frequency: 8.352265134304423e-6
allele num: 119728
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.244-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-120-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-120-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-120-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-120-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-120-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.220-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-69-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-120-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.384-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.244-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-120-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.244-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.308-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.223-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.244-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.220-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-120-7C>A
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-138652C>A
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.244-7C>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

18-55919228-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55919228
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 55919228
    reference: chr 18
allele count: 1
allele frequency: 8.343345347750633e-6
allele num: 119856
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466789
  ensembl transcript: ENST00000588494
  gene symbol: NEDD4L
  hgvsc: ENST00000588494.1:c.-120-5T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256830
  ensembl transcript: ENST00000256830
  gene symbol: NEDD4L
  hgvsc: ENST00000256830.9:c.244-5T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467072
  ensembl transcript: ENST00000586268
  gene symbol: NEDD4L
  hgvsc: ENST00000586268.1:c.-69-5T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000348847
  ensembl transcript: ENST00000356462
  gene symbol: NEDD4L
  hgvsc: ENST00000356462.6:c.244-5T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000466776
  ensembl transcript: ENST00000592846
  gene symbol: NEDD4L
  hgvsc: ENST00000592846.1:c.-120-5T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000372301
  ensembl transcript: ENST00000382850
  gene symbol: NEDD4L
  hgvsc: ENST00000382850.4:c.244-5T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000405440
  ensembl transcript: ENST00000456173
  gene symbol: NEDD4L
  hgvsc: ENST00000456173.2:c.-120-5T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000588066
  gene symbol: NEDD4L
  hgvsc: ENST00000588066.1:n.223-5T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000350569
  ensembl transcript: ENST00000357895
  gene symbol: NEDD4L
  hgvsc: ENST00000357895.5:c.220-5T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000389406
  ensembl transcript: ENST00000431212
  gene symbol: NEDD4L
  hgvsc: ENST00000431212.2:c.-120-5T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000587634
  gene symbol: NEDD4L
  hgvsc: ENST00000587634.1:n.384-5T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000467768
  ensembl transcript: ENST00000587190
  gene symbol: NEDD4L
  hgvsc: ENST00000587190.1:c.-120-5T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000383199
  ensembl transcript: ENST00000400345
  gene symbol: NEDD4L
  hgvsc: ENST00000400345.3:c.244-5T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000468546
  ensembl transcript: ENST00000586263
  gene symbol: NEDD4L
  hgvsc: ENST00000586263.1:c.220-5T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000256832
  ensembl transcript: ENST00000256832
  gene symbol: NEDD4L
  hgvsc: ENST00000256832.7:c.-120-5T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000465669
  ensembl transcript: ENST00000589054
  gene symbol: NEDD4L
  hgvsc: ENST00000589054.1:c.49-138650T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000393395
  ensembl transcript: ENST00000435432
  gene symbol: NEDD4L
  hgvsc: ENST00000435432.2:c.-120-5T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl protein: ENSP00000411947
  ensembl transcript: ENST00000456986
  gene symbol: NEDD4L
  hgvsc: ENST00000456986.1:c.-120-5T>G
  variant of: http://identifiers.org/hgnc/7728
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049759
  ensembl transcript: ENST00000585323
  gene symbol: NEDD4L
  hgvsc: ENST00000585323.1:n.308-5T>G
  variant of: http://identifiers.org/hgnc/7728
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.244-5T>G
num of homozygotes: 0
reference allele: T

GenotypeDepth
all individuals: 923
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 296
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 75
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 361
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2590
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1199
bin: 9.75e1
variant carriers: 25

GenotypeQuality
all individuals: 478
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7187
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39372
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2430
bin: 7.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

South Asian
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allele count: 4
allele frequency: 2.513826043237808e-4
allele num: 15912
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.230920728705071e-4
allele num: 8124
num of homozygotes: 0

European (Non-Finnish)
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allele count: 20
allele frequency: 3.266372693124285e-4
allele num: 61230
num of homozygotes: 0

DP
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QD
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 4.98e-1

BaseQRankSum
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SIO_000300: -1.14e-1

InbreedingCoeff
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SIO_000300: 4.0e-3

MQ
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SIO_000300: 5.95e1

ReadPosRankSum
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SIO_000300: 3.08e-1

ClippingRankSum
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SIO_000300: -1.44e-1

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

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

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.633133002351711e-5
allele num: 61232
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.632386549134835e-5
allele num: 61260
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8126
num of homozygotes: 0

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

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

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

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

QD
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SIO_000300: 9.0e0

ClippingRankSum
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SIO_000300: -3.54e-1

InbreedingCoeff
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SIO_000300: 1.3e-3

MQRankSum
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BaseQRankSum
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SIO_000300: -3.531e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -8.0e-4

MQ
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SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.416128e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-2

GenotypeDepth
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variant carriers: 1

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.26477309826967e-5
allele num: 61260
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.229709788489916e-4
allele num: 8132
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15974
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.74e-1

ClippingRankSum
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FS
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DP
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MQ
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SIO_000300: 5.958e1

MQRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 1.7e-3

QD
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SIO_000300: 1.018e1

ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

Other
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.632120124041129e-5
allele num: 61270
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.264346804204478e-5
allele num: 61268
num of homozygotes: 0

East Asian
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num of homozygotes: 0

European (Finnish)
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African
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Other
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South Asian
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allele num: 15962
num of homozygotes: 0

Latino
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num of homozygotes: 0

FS
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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MQ
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QD
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InbreedingCoeff
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DP
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ReadPosRankSum
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variant carriers: 10

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 3
allele frequency: 3.690036900369004e-4
allele num: 8130
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

South Asian
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allele count: 90
allele frequency: 5.639804486777792e-3
allele num: 15958
num of homozygotes: 2

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61260
num of homozygotes: 0

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

ClippingRankSum
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SIO_000300: -4.8e-2

ReadPosRankSum
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FS
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SIO_000300: 1.212e0

BaseQRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: 9.5e-3

QD
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SIO_000300: 1.242e1

DP
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SIO_000300: 1.414814e6

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8132
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15946
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.220107369448512e-4
allele num: 8196
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61256
num of homozygotes: 0

VQSLOD
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SIO_000300: -2.455e0

BaseQRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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SIO_000300: 2.6e-3

FS
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ReadPosRankSum
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SIO_000300: -8.169999999999999e-1

MQRankSum
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SIO_000300: -3.65e-1

DP
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SIO_000300: 1.412469e6

MQ
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SIO_000300: 5.934e1

GenotypeDepth
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.632972990626735e-5
allele num: 61238
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15916
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e0

FS
type: SiteQuality
SIO_000300: 5.639999999999999e-1

BaseQRankSum
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SIO_000300: 1.88e0

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

QD
type: SiteQuality
SIO_000300: 1.181e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

DP
type: SiteQuality
SIO_000300: 1.408964e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.282985674792661e-5
allele num: 15916
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8128
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61238
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.219809709685289e-4
allele num: 8198
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -6.14e-1

DP
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ClippingRankSum
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SIO_000300: -1.51e0

MQ
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QD
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: 1.88e0

VQSLOD
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SIO_000300: 1.74e0

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 1.219809709685289e-4
allele num: 8198
num of homozygotes: 0

Latino
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allele frequency: 3.540449637103912e-4
allele num: 11298
num of homozygotes: 0

Other
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African
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allele frequency: 3.690036900369004e-4
allele num: 8130
num of homozygotes: 0

European (Finnish)
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allele count: 48
allele frequency: 7.297050775311645e-3
allele num: 6578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 245
allele frequency: 4.000261241550469e-3
allele num: 61246
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South Asian
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allele count: 26
allele frequency: 1.632140615191463e-3
allele num: 15930
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DP
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InbreedingCoeff
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ClippingRankSum
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MQ
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FS
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ReadPosRankSum
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VQSLOD
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QD
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 8130
num of homozygotes: 0

Other
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South Asian
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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QD
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ClippingRankSum
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FS
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MQRankSum
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MQ
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
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European (Finnish)
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South Asian
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African
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Other
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European (Non-Finnish)
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allele frequency: 3.266479388515058e-5
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QD
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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DP
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InbreedingCoeff
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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Latino
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European (Non-Finnish)
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African
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Other
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East Asian
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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MQ
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BaseQRankSum
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VQSLOD
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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South Asian
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Other
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ReadPosRankSum
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DP
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ClippingRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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MQRankSum
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QD
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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European (Non-Finnish)
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South Asian
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European (Finnish)
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East Asian
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DP
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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FS
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MQ
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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European (Non-Finnish)
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South Asian
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European (Finnish)
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QD
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DP
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MQ
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MQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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East Asian
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European (Non-Finnish)
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African
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MQ
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VQSLOD
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FS
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DP
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GenotypeQuality
all individuals: 57
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.634734846007978e-5
allele num: 61172
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15844
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-2

QD
type: SiteQuality
SIO_000300: 1.245e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.17e-1

DP
type: SiteQuality
SIO_000300: 1.368347e6

FS
type: SiteQuality
SIO_000300: 1.851e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.24e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-2

GenotypeDepth
all individuals: 5157
bin: 1.75e1
variant carriers: 12

GenotypeDepth
all individuals: 109
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28695
bin: 2.25e1
variant carriers: 16

GenotypeDepth
all individuals: 4944
bin: 3.25e1
variant carriers: 11

GenotypeDepth
all individuals: 1291
bin: 3.75e1
variant carriers: 8

GenotypeDepth
all individuals: 96
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2025
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1222
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 9.75e1
variant carriers: 70

GenotypeQuality
all individuals: 2278
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6422
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 60
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31818
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2445
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1357
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.770538243626062e-4
allele num: 11296
num of homozygotes: 0

South Asian
type: Population
allele count: 54
allele frequency: 3.409952008082849e-3
allele num: 15836
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 6.103515625e-4
allele num: 8192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.797385620915033e-4
allele num: 61200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8118
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

DP
type: SiteQuality
SIO_000300: 1.362919e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

FS
type: SiteQuality
SIO_000300: 1.643e0

QD
type: SiteQuality
SIO_000300: 1.412e1

MQRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 959
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 243
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1282
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 504
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1740
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2188
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1383
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30262
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1365
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2275
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1200
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1210
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 700
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6354
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2449
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 834
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1700
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2286
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11290
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15816
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.634200549091385e-5
allele num: 61192
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.49e-1

QD
type: SiteQuality
SIO_000300: 5.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e-1

DP
type: SiteQuality
SIO_000300: 1.359939e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: -1.857e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.767e1

GenotypeDepth
all individuals: 3799
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 385
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1334
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15007
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 413
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 219
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31110
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 410
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2108
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 734
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10826
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4919
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26928
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1982
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4009
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2496
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3003
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1698
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7684
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.970055161544523e-4
allele num: 10152
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.7e-1

DP
type: SiteQuality
SIO_000300: 5.91537e5

FS
type: SiteQuality
SIO_000300: 1.33e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

VQSLOD
type: SiteQuality
SIO_000300: -4.131e-1

QD
type: SiteQuality
SIO_000300: 1.046e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.13e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.06e-1

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000049759
ensembl protein: ENSP00000466789
ensembl transcript: ENST00000588494
gene symbol: NEDD4L
hgvsc: ENST00000588494.1:c.-241-3C>T
variant of: http://identifiers.org/hgnc/7728

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000049759
ensembl protein: ENSP00000389406
ensembl transcript: ENST00000431212
gene symbol: NEDD4L
hgvsc: ENST00000431212.2:c.-241-3C>T
variant of: http://identifiers.org/hgnc/7728

GenotypeDepth
all individuals: 2377
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33045
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1485
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 386
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 181
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5709
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13096
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 218
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 764
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 416
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7129
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3000
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12695
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1254
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 253
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31417
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 703
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 421
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2756
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8014
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1880
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.098e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.41e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.203e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

QD
type: SiteQuality
SIO_000300: 5.34e0

DP
type: SiteQuality
SIO_000300: 7.27456e5

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000049759
ensembl transcript: ENST00000591989
gene symbol: NEDD4L
hgvsc: ENST00000591989.1:n.177G>A
variant of: http://identifiers.org/hgnc/7728

GenotypeDepth
all individuals: 8718
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 218
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6990
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 378
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 387
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 413
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 403
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1890
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 35591
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2485
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 769
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8330
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3006
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 261
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 929
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34223
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8519
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 250
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 302
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1354
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1542
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2058
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.757669955399378e-5
allele num: 14798
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.635578583765112e-4
allele num: 1158
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3188
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8216
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.48e-1

QD
type: SiteQuality
SIO_000300: 1.237e1

FS
type: SiteQuality
SIO_000300: 1.584e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.25e-1

DP
type: SiteQuality
SIO_000300: 7.73847e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.52e-2

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000049759
ensembl transcript: ENST00000585363
gene symbol: NEDD4L
hgvsc: ENST00000585363.1:n.166G>T
variant of: http://identifiers.org/hgnc/7728

GenotypeDepth
all individuals: 35591
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 8718
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 387
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 378
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 403
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2485
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 769
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 218
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6990
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1890
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 471
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 413
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34223
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8330
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 302
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3006
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 929
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8519
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1354
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14798
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8216
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2058
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 6.273525721455458e-4
allele num: 3188
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727115716753022e-3
allele num: 1158
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.584e0

QD
type: SiteQuality
SIO_000300: 1.237e1

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.52e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.25e-1

DP
type: SiteQuality
SIO_000300: 7.73847e5

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000049759
ensembl transcript: ENST00000585323
gene symbol: NEDD4L
hgvsc: ENST00000585323.1:n.197G>C
variant of: http://identifiers.org/hgnc/7728

GenotypeDepth
all individuals: 471
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7485
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7706
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 387
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 218
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2502
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36014
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 403
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 412
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1978
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 88
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7345
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9033
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1238
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 492
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34911
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 161
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3386
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1784
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.295643414756988e-5
allele num: 15884
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2160
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

DP
type: SiteQuality
SIO_000300: 7.91072e5

QD
type: SiteQuality
SIO_000300: 9.35e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 3.7e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.243e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

GenotypeDepth
all individuals: 218
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2551
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2130
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 413
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36101
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 403
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 448
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5938
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8946
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 776
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 386
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5853
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35379
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 96
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10238
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 328
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.653550429669833e-5
allele num: 17688
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3682
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2274
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.007e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.789e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.26e-2

DP
type: SiteQuality
SIO_000300: 8.18152e5

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.05e-1

QD
type: SiteQuality
SIO_000300: 6.8e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000049759
ensembl protein: ENSP00000411947
ensembl transcript: ENST00000456986
gene symbol: NEDD4L
hgvsc: ENST00000456986.1:c.-214C>T
variant of: http://identifiers.org/hgnc/7728

GenotypeDepth
all individuals: 4383
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 386
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10813
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35310
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 403
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 413
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2384
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 561
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 790
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 218
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2668
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 263
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3002
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4356
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1058
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35037
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11914
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2028
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2656
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20342
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.302555836979047e-4
allele num: 8686
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4146
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

DP
type: SiteQuality
SIO_000300: 8.57457e5

MQRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

QD
type: SiteQuality
SIO_000300: 8.67e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000049759
ensembl transcript: ENST00000585323
gene symbol: NEDD4L
hgvsc: ENST00000585323.1:n.220G>A
variant of: http://identifiers.org/hgnc/7728

GenotypeDepth
all individuals: 11744
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 403
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 795
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2793
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34519
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 3817
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 218
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 386
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 416
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 618
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2629
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12963
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 283
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34843
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3814
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 252
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2296
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21750
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8890
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2936
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-2

QD
type: SiteQuality
SIO_000300: 4.24e0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

FS
type: SiteQuality
SIO_000300: 1.027e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.88e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.697e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.29e-1

DP
type: SiteQuality
SIO_000300: 8.78079e5

MQ
type: SiteQuality
SIO_000300: 5.915e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000049759
ensembl transcript: ENST00000588066
gene symbol: NEDD4L
hgvsc: ENST00000588066.1:n.139G>A
variant of: http://identifiers.org/hgnc/7728

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2900
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 34098
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 218
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 606
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2848
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3781
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11891
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 403
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 386
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 414
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 796
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12825
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3775
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34538
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1038
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1066
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 106
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8950
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2700
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3050
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.205558006175562e-4
allele num: 4534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.82978e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.95e-1

FS
type: SiteQuality
SIO_000300: 2.749e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.214e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.5e-1

QD
type: SiteQuality
SIO_000300: 9.26e0

VQSLOD
type: SiteQuality
SIO_000300: 5.48e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.4e-3

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000049759
ensembl transcript: ENST00000588066
gene symbol: NEDD4L
hgvsc: ENST00000588066.1:n.142A>G
variant of: http://identifiers.org/hgnc/7728

GenotypeDepth
all individuals: 244
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2992
bin: 1.25e1
variant carriers: 8

GenotypeDepth
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12187
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 386
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33898
bin: 7.5e0
variant carriers: 3

GenotypeDepth
all individuals: 786
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 403
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 218
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 538
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3650
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 413
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2877
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 225
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3643
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34782
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13491
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 164
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3012
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 350
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 1.80635838150289e-3
allele num: 2768
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 3.056234718826406e-4
allele num: 22904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3138
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 7.898894154818325e-4
allele num: 2532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9004
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.223e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.699999999999999e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.8e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

FS
type: SiteQuality
SIO_000300: 1.75e0

DP
type: SiteQuality
SIO_000300: 8.88119e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

GenotypeDepth
all individuals: 2827
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7759
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 218
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 706
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6882
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 416
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31038
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 794
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6802
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 405
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 386
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 644
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7990
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1506
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33855
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 8600
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2242
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21354
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2778
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 362
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8796
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.63e-2

DP
type: SiteQuality
SIO_000300: 8.14587e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQ
type: SiteQuality
SIO_000300: 5.018e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.307e0

QD
type: SiteQuality
SIO_000300: 7.66e0

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeDepth
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 413
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 386
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7020
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6455
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8638
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 714
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2727
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30451
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 218
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 783
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33038
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8895
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1751
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3001
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 296
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8017
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8720
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 362
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2720
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4136
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.765535646206634e-5
allele num: 20984
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.633e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.78e-2

QD
type: SiteQuality
SIO_000300: 1.038e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.397e0

MQRankSum
type: SiteQuality
SIO_000300: -1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e-1

DP
type: SiteQuality
SIO_000300: 8.02998e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.04e-1

GenotypeDepth
all individuals: 5041
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 778
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 387
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 403
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12878
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 649
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7530
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 414
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27218
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 218
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1074
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13189
bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 5.097359567743908e-5
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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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African
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ReadPosRankSum
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QD
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DP
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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FS
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MQRankSum
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MQ
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ClippingRankSum
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variant carriers: 1

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

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

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

DP
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FS
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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MQ
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VQSLOD
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BaseQRankSum
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SIO_000300: 2.96e-1

ReadPosRankSum
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SIO_000300: -5.46e-1

QD
type: SiteQuality
SIO_000300: 1.123e1

GenotypeDepth
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variant carriers: 0

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

African
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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African
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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: 0.0e0
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South Asian
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Other
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MQRankSum
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ClippingRankSum
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DP
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ReadPosRankSum
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VQSLOD
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FS
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InbreedingCoeff
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MQ
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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African
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Other
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East Asian
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South Asian
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European (Finnish)
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ClippingRankSum
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InbreedingCoeff
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FS
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MQRankSum
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MQ
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VQSLOD
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BaseQRankSum
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DP
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SIO_000300: 6.24891e5

QD
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SIO_000300: 1.671e1

ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

South Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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European (Finnish)
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African
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Other
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ReadPosRankSum
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SIO_000300: -1.146e0

InbreedingCoeff
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QD
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VQSLOD
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FS
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SIO_000300: 9.26e-1

ClippingRankSum
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MQRankSum
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MQ
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SIO_000300: 5.958e1

BaseQRankSum
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SIO_000300: 4.16e0

DP
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GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.075268817204301e-4
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African
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
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MQ
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SIO_000300: 6.0e1

VQSLOD
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DP
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SIO_000300: 6.23225e5

BaseQRankSum
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MQRankSum
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InbreedingCoeff
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SIO_000300: -6.98e-2

FS
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SIO_000300: 6.107e0

ReadPosRankSum
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SIO_000300: 1.81e-1

ClippingRankSum
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SIO_000300: 1.81e-1

GenotypeDepth
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variant carriers: 0

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

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

European (Finnish)
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Other
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allele count: 0
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Latino
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allele count: 0
allele frequency: 0.0e0
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African
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East Asian
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South Asian
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allele count: 2
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -6.87e-2

FS
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SIO_000300: 3.071e0

DP
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ReadPosRankSum
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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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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

Latino
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South Asian
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European (Non-Finnish)
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East Asian
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European (Finnish)
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num of homozygotes: 0

Other
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FS
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InbreedingCoeff
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DP
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QD
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VQSLOD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
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num of homozygotes: 0

East Asian
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European (Finnish)
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South Asian
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Other
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num of homozygotes: 0

Latino
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InbreedingCoeff
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FS
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DP
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MQ
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QD
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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African
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MQ
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FS
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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Latino
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East Asian
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African
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South Asian
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MQ
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InbreedingCoeff
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ClippingRankSum
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FS
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QD
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ReadPosRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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African
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European (Finnish)
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East Asian
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Other
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Latino
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DP
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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FS
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VQSLOD
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ReadPosRankSum
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QD
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MQ
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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South Asian
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East Asian
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European (Non-Finnish)
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BaseQRankSum
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FS
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MQRankSum
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QD
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ReadPosRankSum
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VQSLOD
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Other
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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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MQRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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MQ
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 2.538071065989848e-3
allele num: 394
num of homozygotes: 0

South 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 count: 0
allele frequency: 0.0e0
allele num: 8776
num of homozygotes: 0

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

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

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

South Asian
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num of homozygotes: 0

Other
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allele count: 0
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num of homozygotes: 0

African
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allele count: 1
allele frequency: 4.578754578754579e-4
allele num: 2184
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1622
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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InbreedingCoeff
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SIO_000300: -7.770000000000001e-2

BaseQRankSum
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SIO_000300: 5.41e0

ClippingRankSum
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SIO_000300: 7.27e-1

QD
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SIO_000300: 1.633e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1622
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.345765892563922e-4
allele num: 8526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.651e0

ClippingRankSum
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SIO_000300: 6.76e-1

QD
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SIO_000300: 1.225e1

MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.47e0

DP
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SIO_000300: 5.01609e5

BaseQRankSum
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SIO_000300: 5.52e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.15e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.92e-1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

Other
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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
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num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.655629139072848e-3
allele num: 604
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 8416
num of homozygotes: 0

DP
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SIO_000300: 4.99124e5

QD
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VQSLOD
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MQ
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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FS
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BaseQRankSum
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SIO_000300: -3.142e0

GenotypeDepth
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variant carriers: 19

GenotypeDepth
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GenotypeDepth
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variant carriers: 27

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

European (Finnish)
type: Population
allele count: 18
allele frequency: 2.752293577981652e-3
allele num: 6540
num of homozygotes: 0

South Asian
type: Population
allele count: 126
allele frequency: 7.746219107340465e-3
allele num: 16266
num of homozygotes: 1

African
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allele count: 5
allele frequency: 5.324813631522897e-4
allele num: 9390
num of homozygotes: 0

Latino
type: Population
allele count: 16
allele frequency: 1.420706801633813e-3
allele num: 11262
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

European (Non-Finnish)
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allele count: 317
allele frequency: 4.858833266913951e-3
allele num: 65242
num of homozygotes: 2

Other
type: Population
allele count: 4
allele frequency: 4.576659038901602e-3
allele num: 874
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FS
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SIO_000300: 9.27e-1

ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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ClippingRankSum
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DP
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VQSLOD
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MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 1.43e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 450
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GenotypeQuality
all individuals: 23360
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65400
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.659574468085106e-4
allele num: 11280
num of homozygotes: 0

East Asian
type: Population
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allele frequency: 0.0e0
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African
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Other
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ClippingRankSum
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VQSLOD
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DP
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MQ
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ReadPosRankSum
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QD
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FS
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MQRankSum
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SIO_000300: -2.9e-2

BaseQRankSum
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SIO_000300: -3.031e0

InbreedingCoeff
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SIO_000300: -4.0e-4

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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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allele num: 9418
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Other
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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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ReadPosRankSum
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VQSLOD
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MQRankSum
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FS
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QD
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.583791712504584e-5
allele num: 65448
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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Other
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BaseQRankSum
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SIO_000300: 2.49e0

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

European (Finnish)
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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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South Asian
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Other
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African
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allele count: 0
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Latino
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allele frequency: 2.649708532061473e-4
allele num: 11322
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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FS
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InbreedingCoeff
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QD
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VQSLOD
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BaseQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65880
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Latino
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allele frequency: 8.795074758135444e-5
allele num: 11370
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South Asian
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European (Finnish)
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African
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Other
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East Asian
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MQ
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VQSLOD
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ClippingRankSum
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QD
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FS
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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African
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Latino
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European (Non-Finnish)
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MQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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DP
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

QD
type: SiteQuality
SIO_000300: 1.608e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.115e0

GenotypeDepth
all individuals: 518
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 500
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2468
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7292
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 746
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2791
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1439
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14034
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2012
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1064
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 140
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21857
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 502
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 277
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3942
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 353
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1513
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29516
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6144
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3082
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2379
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12922
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1181
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2305
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510345869204048e-5
allele num: 66210
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9586
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e0

QD
type: SiteQuality
SIO_000300: 1.288e1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

DP
type: SiteQuality
SIO_000300: 2.194132e6

VQSLOD
type: SiteQuality
SIO_000300: 7.33e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

FS
type: SiteQuality
SIO_000300: 1.054e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.63e-1

GenotypeDepth
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2468
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14073
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 277
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1064
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2790
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 746
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 443
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 423
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2012
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 518
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21989
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3943
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7284
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 353
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1439
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 138
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12923
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 160
bin: 3.25e1
variant carriers: 0