17-80441675-AGAGTCCTCTGGGGG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80441675
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80441661
    reference: chr 17
allele count: 1
allele frequency: 8.273077750384698e-6
allele num: 120874
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000463087
  ensembl transcript: ENST00000581795
  gene symbol: NARF
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000409710
  ensembl transcript: ENST00000412079
  gene symbol: NARF
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462305
  ensembl transcript: ENST00000581202
  gene symbol: NARF
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: AGAGTCCTCTGGGGG
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-80441682-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80441682
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80441682
    reference: chr 17
allele count: 5
allele frequency: 4.139826789647121e-5
allele num: 120778
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*363+27T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+64T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.195+27T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.698+27T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000409710
  ensembl transcript: ENST00000412079
  gene symbol: NARF
  hgvsc: ENST00000412079.2:c.*23T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000463087
  ensembl transcript: ENST00000581795
  gene symbol: NARF
  hgvsc: ENST00000581795.1:c.*390T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.971+27T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.952T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.833+27T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.656+27T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.835T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*182+27T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.689+27T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462305
  ensembl transcript: ENST00000581202
  gene symbol: NARF
  hgvsc: ENST00000581202.1:c.*209T>C
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4605
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15634
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/17-80441683-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80441683
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80441683
    reference: chr 17
allele count: 3
allele frequency: 2.484595507851322e-5
allele num: 120744
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.971+28C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.698+28C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462305
  ensembl transcript: ENST00000581202
  gene symbol: NARF
  hgvsc: ENST00000581202.1:c.*210C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.195+28C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000463087
  ensembl transcript: ENST00000581795
  gene symbol: NARF
  hgvsc: ENST00000581795.1:c.*391C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.656+28C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+65C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000409710
  ensembl transcript: ENST00000412079
  gene symbol: NARF
  hgvsc: ENST00000412079.2:c.*24C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.689+28C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*363+28C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.836C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.953C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.833+28C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*182+28C>A
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15737
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

17-80441684-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80441684
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80441685
    reference: chr 17
allele count: 2
allele frequency: 1.658044833532299e-5
allele num: 120624
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.971+35dupG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462305
  ensembl transcript: ENST00000581202
  gene symbol: NARF
  hgvsc: ENST00000581202.1:c.*217dupG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*182+35dupG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000409710
  ensembl transcript: ENST00000412079
  gene symbol: NARF
  hgvsc: ENST00000412079.2:c.*31dupG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.843dupG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.656+35dupG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.833+35dupG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*363+35dupG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000463087
  ensembl transcript: ENST00000581795
  gene symbol: NARF
  hgvsc: ENST00000581795.1:c.*398dupG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.960dupG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+72dupG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.195+35dupG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.698+35dupG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.689+35dupG
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15516
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

17-80441685-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80441685
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80441685
    reference: chr 17
allele count: 11
allele frequency: 9.121666445535359e-5
allele num: 120592
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*363+30G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.955G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.838G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000409710
  ensembl transcript: ENST00000412079
  gene symbol: NARF
  hgvsc: ENST00000412079.2:c.*26G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.833+30G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.195+30G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+67G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462305
  ensembl transcript: ENST00000581202
  gene symbol: NARF
  hgvsc: ENST00000581202.1:c.*212G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.656+30G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.698+30G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.689+30G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000463087
  ensembl transcript: ENST00000581795
  gene symbol: NARF
  hgvsc: ENST00000581795.1:c.*393G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.971+30G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*182+30G>C
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15616
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

17-80441686-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80441686
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80441686
    reference: chr 17
allele count: 1
allele frequency: 8.285278716776033e-6
allele num: 120696
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000463087
  ensembl transcript: ENST00000581795
  gene symbol: NARF
  hgvsc: ENST00000581795.1:c.*394G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000409710
  ensembl transcript: ENST00000412079
  gene symbol: NARF
  hgvsc: ENST00000412079.2:c.*27G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.971+31G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+68G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.833+31G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*363+31G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.656+31G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.689+31G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.956G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462305
  ensembl transcript: ENST00000581202
  gene symbol: NARF
  hgvsc: ENST00000581202.1:c.*213G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.839G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*182+31G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.698+31G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.195+31G>A
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

17-80441686-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80441686
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80441686
    reference: chr 17
allele count: 1
allele frequency: 8.285278716776033e-6
allele num: 120696
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.839G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+68G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.971+31G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.956G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.698+31G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462305
  ensembl transcript: ENST00000581202
  gene symbol: NARF
  hgvsc: ENST00000581202.1:c.*213G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*182+31G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.833+31G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000463087
  ensembl transcript: ENST00000581795
  gene symbol: NARF
  hgvsc: ENST00000581795.1:c.*394G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000409710
  ensembl transcript: ENST00000412079
  gene symbol: NARF
  hgvsc: ENST00000412079.2:c.*27G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.656+31G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.195+31G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*363+31G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.689+31G>C
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4558
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP

17-80441687-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80441687
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80441687
    reference: chr 17
allele count: 1
allele frequency: 8.284043275842073e-6
allele num: 120714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*363+32G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.195+32G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.833+32G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000463087
  ensembl transcript: ENST00000581795
  gene symbol: NARF
  hgvsc: ENST00000581795.1:c.*395G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.698+32G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.957G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000409710
  ensembl transcript: ENST00000412079
  gene symbol: NARF
  hgvsc: ENST00000412079.2:c.*28G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.689+32G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*182+32G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.971+32G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462305
  ensembl transcript: ENST00000581202
  gene symbol: NARF
  hgvsc: ENST00000581202.1:c.*214G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.656+32G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+69G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.840G>A
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5811
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

17-80441689-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80441689
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80441689
    reference: chr 17
allele count: 1
allele frequency: 8.285827919925758e-6
allele num: 120688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.689+34G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.195+34G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.842G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*363+34G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000463087
  ensembl transcript: ENST00000581795
  gene symbol: NARF
  hgvsc: ENST00000581795.1:c.*397G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.959G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000409710
  ensembl transcript: ENST00000412079
  gene symbol: NARF
  hgvsc: ENST00000412079.2:c.*30G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+71G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.656+34G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462305
  ensembl transcript: ENST00000581202
  gene symbol: NARF
  hgvsc: ENST00000581202.1:c.*216G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*182+34G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.833+34G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.698+34G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.971+34G>A
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9246
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5805
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  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: Other
population: African
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

17-80441692-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80441692
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80441692
    reference: chr 17
allele count: 4
allele frequency: 3.316639580776757e-5
allele num: 120604
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.698+37A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.962A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000463087
  ensembl transcript: ENST00000581795
  gene symbol: NARF
  hgvsc: ENST00000581795.1:c.*400A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000409710
  ensembl transcript: ENST00000412079
  gene symbol: NARF
  hgvsc: ENST00000412079.2:c.*33A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.971+37A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462305
  ensembl transcript: ENST00000581202
  gene symbol: NARF
  hgvsc: ENST00000581202.1:c.*219A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.845A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.656+37A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.195+37A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.689+37A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*363+37A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*182+37A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.833+37A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+74A>G
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/17-80441701-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80441701
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80441701
    reference: chr 17
allele count: 1
allele frequency: 8.320021299254527e-6
allele num: 120192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000463087
  ensembl transcript: ENST00000581795
  gene symbol: NARF
  hgvsc: ENST00000581795.1:c.*409C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.195+46C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.854C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.971+46C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*363+46C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.689+46C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000409710
  ensembl transcript: ENST00000412079
  gene symbol: NARF
  hgvsc: ENST00000412079.2:c.*42C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.698+46C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.971C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*182+46C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.656+46C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+83C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.833+46C>A
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12882
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8611
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum

17-80441701-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80441701
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80441701
    reference: chr 17
allele count: 2
allele frequency: 1.664004259850905e-5
allele num: 120192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+83C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.698+46C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.195+46C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000463087
  ensembl transcript: ENST00000581795
  gene symbol: NARF
  hgvsc: ENST00000581795.1:c.*409C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.689+46C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.833+46C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*363+46C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000409710
  ensembl transcript: ENST00000412079
  gene symbol: NARF
  hgvsc: ENST00000412079.2:c.*42C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.971C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.656+46C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*182+46C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.854C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.971+46C>T
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6922
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8611
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

17-80441702-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80441702
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80441702
    reference: chr 17
allele count: 6
allele frequency: 4.999333422210372e-5
allele num: 120016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.971+47G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.689+47G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.855G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*363+47G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*182+47G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000409710
  ensembl transcript: ENST00000412079
  gene symbol: NARF
  hgvsc: ENST00000412079.2:c.*43G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.833+47G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.195+47G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.972G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000463087
  ensembl transcript: ENST00000581795
  gene symbol: NARF
  hgvsc: ENST00000581795.1:c.*410G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.656+47G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.698+47G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+84G>A
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7455
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/17-80442646-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442646
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442646
    reference: chr 17
allele count: 1
allele frequency: 8.911226362972073e-6
allele num: 112218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.690-43C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1799C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.834-43C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1916C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.657-43C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1028C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.699-43C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*183-43C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.232C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-727C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.972-43C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*364-43C>A
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3151
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5630
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4091
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7272
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-80442646-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442646
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442646
    reference: chr 17
allele count: 5
allele frequency: 4.455613181486036e-5
allele num: 112218
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.232C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1799C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1028C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.972-43C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*183-43C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.690-43C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-727C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.657-43C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1916C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.834-43C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.699-43C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*364-43C>T
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8216
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5630
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6555
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-80442647-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442647
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442647
    reference: chr 17
allele count: 592
allele frequency: 5.272063407249087e-3
allele num: 112290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1029G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.690-42G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*364-42G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.699-42G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1800G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.834-42G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-726G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*183-42G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1917G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.657-42G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.233G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.972-42G>A
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8217
  bin: 4.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 7851
  bin: 3.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6520
  bin: 3.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 6.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 7280
  bin: 4.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 7.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 6.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 4099
  bin: 5.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 5626
  bin: 5.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 2.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 9.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 7.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 8.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
num of homozygotes: 18
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/17-80442656-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442656
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442656
    reference: chr 17
allele count: 1
allele frequency: 8.885887433577992e-6
allele num: 112538
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.690-33C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1809C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.972-33C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.657-33C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.834-33C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*364-33C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.242C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-717C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1038C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1926C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.699-33C>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*183-33C>A
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6542
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

17-80442670-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442670
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442670
    reference: chr 17
allele count: 15
allele frequency: 1.324199300822769e-4
allele num: 113276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.972-19A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*183-19A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.256A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1940A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1823A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*364-19A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.690-19A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.834-19A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-703A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.657-19A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1052A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.699-19A>G
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4096
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8224
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7862
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum

17-80442673-TTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442673
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442671
    reference: chr 17
allele count: 1
allele frequency: 8.817564588660612e-6
allele num: 113410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*364-12_*364-11delCT
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1947_1948delCT
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-696_196-695delCT
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.699-12_699-11delCT
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.263_264delCT
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.690-12_690-11delCT
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.834-12_834-11delCT
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1059_240+1060delCT
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1830_1831delCT
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*183-12_*183-11delCT
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.657-12_657-11delCT
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.972-12_972-11delCT
  variant of: http://identifiers.org/hgnc/29916
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4096
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8224
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3554
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: TTC
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD

17-80442683-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442683
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442683
    reference: chr 17
allele count: 4127
allele frequency: 3.582589673252543e-2
allele num: 115196
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1953T>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*364-6T>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.699-6T>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1836T>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.269T>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1065T>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.972-6T>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.834-6T>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.690-6T>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.657-6T>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-690T>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*183-6T>G
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 1.25e1
  variant carriers: 181
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.75e1
  variant carriers: 236
genotype depth: GenotypeDepth
  all individuals: 7852
  bin: 4.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6273
  bin: 3.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 2.25e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 4092
  bin: 2.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 7492
  bin: 3.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 257
genotype depth: GenotypeDepth
  all individuals: 6940
  bin: 4.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 7.5e0
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.75e1
  variant carriers: 187
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 6.75e1
  variant carriers: 254
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.25e1
  variant carriers: 286
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 5.75e1
  variant carriers: 183
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 7.75e1
  variant carriers: 271
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 9.75e1
  variant carriers: 1137
genotype quality: GenotypeQuality
hgvs: c.834-6T>G
num of homozygotes: 93
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum

17-80442684-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442684
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442684
    reference: chr 17
allele count: 2
allele frequency: 1.734003814808392e-5
allele num: 115340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.972-5G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*364-5G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*183-5G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.270G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-689G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.834-5G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1954G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.699-5G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1837G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.690-5G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1066G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.657-5G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.1G>C
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4010
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7861
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.834-5G>C
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-80442686-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442686
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442686
    reference: chr 17
allele count: 2
allele frequency: 1.730343300110742e-5
allele num: 115584
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.972-3G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.699-3G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*364-3G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1068G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1839G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.3G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*183-3G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.834-3G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.690-3G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1956G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-687G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.657-3G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.272G>A
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4010
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6258
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.834-3G>A
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

17-80442687-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442687
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442686
    reference: chr 17
allele count: 1
allele frequency: 8.64902266043937e-6
allele num: 115620
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1842delG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1959delG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.699delG
  hgvsp: ENSP00000462792.1:p.Phe234LeufsTer4
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.275delG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*183delG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.834delG
  hgvsp: ENSP00000309899.10:p.Phe279LeufsTer4
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.657delG
  hgvsp: ENSP00000374656.4:p.Phe220LeufsTer4
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*364delG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.972delG
  hgvsp: ENSP00000414678.3:p.Phe325LeufsTer4
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.690delG
  hgvsp: ENSP00000283996.9:p.Phe231LeufsTer4
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.6delG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-684delG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1071delG
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4010
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.834delG
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: AG
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

17-80442689-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442689
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442689
    reference: chr 17
allele count: 2
allele frequency: 1.725089704664643e-5
allele num: 115936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.690G>A
  hgvsp: ENST00000345415.7:c.690G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.6G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1071G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*364G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.972G>A
  hgvsp: ENST00000457415.3:c.972G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.275G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.657G>A
  hgvsp: ENST00000390006.4:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*183G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1959G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1842G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-684G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.699G>A
  hgvsp: ENST00000577432.1:c.699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.834G>A
  hgvsp: ENST00000309794.11:c.834G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6948
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.834G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS

17-80442693-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442693
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442693
    reference: chr 17
allele count: 1
allele frequency: 8.592246356887545e-6
allele num: 116384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1075G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.661G>A
  hgvsp: ENSP00000374656.4:p.Gly221Arg
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*368G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.694G>A
  hgvsp: ENSP00000283996.9:p.Gly232Arg
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*187G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.10G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.976G>A
  hgvsp: ENSP00000414678.3:p.Gly326Arg
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.838G>A
  hgvsp: ENSP00000309899.10:p.Gly280Arg
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1963G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.279G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.703G>A
  hgvsp: ENSP00000462792.1:p.Gly235Arg
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-680G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1846G>A
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4010
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6947
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly280Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS

17-80442698-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442698
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442698
    reference: chr 17
allele count: 1
allele frequency: 8.546132020647455e-6
allele num: 117012
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.666C>G
  hgvsp: ENSP00000374656.4:p.Asp222Glu
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1080C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.981C>G
  hgvsp: ENSP00000414678.3:p.Asp327Glu
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1968C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.699C>G
  hgvsp: ENSP00000283996.9:p.Asp233Glu
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1851C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.843C>G
  hgvsp: ENSP00000309899.10:p.Asp281Glu
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.708C>G
  hgvsp: ENSP00000462792.1:p.Asp236Glu
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*192C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.284C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-675C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.15C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*373C>G
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7862
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp281Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum

17-80442700-TGAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442700
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442697
    reference: chr 17
allele count: 8
allele frequency: 6.814890535820769e-5
allele num: 117390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.288_290delAAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1972_1974delAAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.985_987delAAG
  hgvsp: ENSP00000414678.3:p.Lys329del
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*377_*379delAAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.703_705delAAG
  hgvsp: ENSP00000283996.9:p.Lys235del
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.712_714delAAG
  hgvsp: ENSP00000462792.1:p.Lys238del
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.670_672delAAG
  hgvsp: ENSP00000374656.4:p.Lys224del
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1855_1857delAAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1084_240+1086delAAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.847_849delAAG
  hgvsp: ENSP00000309899.10:p.Lys283del
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.19_21delAAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*196_*198delAAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-671_196-669delAAG
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6948
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys283del
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: TGAA
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

17-80442702-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442702
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442702
    reference: chr 17
allele count: 1
allele frequency: 8.501810885718658e-6
allele num: 117622
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*196A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1084A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1855A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.847A>G
  hgvsp: ENSP00000309899.10:p.Lys283Glu
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1972A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.19A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.985A>G
  hgvsp: ENSP00000414678.3:p.Lys329Glu
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.712A>G
  hgvsp: ENSP00000462792.1:p.Lys238Glu
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.703A>G
  hgvsp: ENSP00000283996.9:p.Lys235Glu
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*377A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-671A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.670A>G
  hgvsp: ENSP00000374656.4:p.Lys224Glu
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.288A>G
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6947
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7860
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6284
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys283Glu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

17-80442707-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442707
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442707
    reference: chr 17
allele count: 1
allele frequency: 8.454228805248384e-6
allele num: 118284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-666G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*201G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*382G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.708G>A
  hgvsp: ENST00000345415.7:c.708G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1977G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.24G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.852G>A
  hgvsp: ENST00000309794.11:c.852G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.990G>A
  hgvsp: ENST00000457415.3:c.990G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1860G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.675G>A
  hgvsp: ENST00000390006.4:c.675G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.717G>A
  hgvsp: ENST00000577432.1:c.717G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.293G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1089G>A
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7860
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu284Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

17-80442707-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442707
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442707
    reference: chr 17
allele count: 10
allele frequency: 8.454228805248385e-5
allele num: 118284
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.990G>C
  hgvsp: ENSP00000414678.3:p.Glu330Asp
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1860G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.675G>C
  hgvsp: ENSP00000374656.4:p.Glu225Asp
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.293G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-666G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1089G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.708G>C
  hgvsp: ENSP00000283996.9:p.Glu236Asp
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.24G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*382G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.852G>C
  hgvsp: ENSP00000309899.10:p.Glu284Asp
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*201G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1977G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.717G>C
  hgvsp: ENSP00000462792.1:p.Glu239Asp
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7860
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Glu284Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-80442718-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442718
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442718
    reference: chr 17
allele count: 3
allele frequency: 2.512562814070352e-5
allele num: 119400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.35C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.686C>T
  hgvsp: ENSP00000374656.4:p.Thr229Met
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1871C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-655C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.719C>T
  hgvsp: ENSP00000283996.9:p.Thr240Met
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*212C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.728C>T
  hgvsp: ENSP00000462792.1:p.Thr243Met
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*393C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1988C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1001C>T
  hgvsp: ENSP00000414678.3:p.Thr334Met
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.863C>T
  hgvsp: ENSP00000309899.10:p.Thr288Met
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.304C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1100C>T
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr288Met
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD

17-80442718-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442718
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442717
    reference: chr 17
allele count: 1
allele frequency: 8.375209380234507e-6
allele num: 119400
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.864delG
  hgvsp: ENSP00000309899.10:p.Arg289ValfsTer35
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1872delG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*394delG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.687delG
  hgvsp: ENSP00000374656.4:p.Arg230ValfsTer35
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1002delG
  hgvsp: ENSP00000414678.3:p.Arg335ValfsTer35
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.305delG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*213delG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.36delG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-654delG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1989delG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.729delG
  hgvsp: ENSP00000462792.1:p.Arg244ValfsTer?
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.720delG
  hgvsp: ENSP00000283996.9:p.Arg241ValfsTer35
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1101delG
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg289ValfsTer35
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: CG
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

17-80442719-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442719
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442719
    reference: chr 17
allele count: 2
allele frequency: 1.67266036631262e-5
allele num: 119570
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.305G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1002G>A
  hgvsp: ENST00000457415.3:c.1002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1101G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.687G>A
  hgvsp: ENST00000390006.4:c.687G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*213G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.864G>A
  hgvsp: ENST00000309794.11:c.864G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1872G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.720G>A
  hgvsp: ENST00000345415.7:c.720G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.36G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*394G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-654G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.729G>A
  hgvsp: ENST00000577432.1:c.729G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1989G>A
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5409
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr288Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-80442720-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442720
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442720
    reference: chr 17
allele count: 2
allele frequency: 1.671206778414693e-5
allele num: 119674
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.865C>T
  hgvsp: ENSP00000309899.10:p.Arg289Cys
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1102C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.37C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.721C>T
  hgvsp: ENSP00000283996.9:p.Arg241Cys
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.688C>T
  hgvsp: ENSP00000374656.4:p.Arg230Cys
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1990C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*395C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1003C>T
  hgvsp: ENSP00000414678.3:p.Arg335Cys
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*214C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.306C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.730C>T
  hgvsp: ENSP00000462792.1:p.Arg244Cys
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1873C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-653C>T
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg289Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

17-80442721-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442721
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442721
    reference: chr 17
allele count: 29
allele frequency: 2.420781996059969e-4
allele num: 119796
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*396G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.307G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-652G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.689G>A
  hgvsp: ENSP00000374656.4:p.Arg230His
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.731G>A
  hgvsp: ENSP00000462792.1:p.Arg244His
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.38G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.866G>A
  hgvsp: ENSP00000309899.10:p.Arg289His
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.722G>A
  hgvsp: ENSP00000283996.9:p.Arg241His
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1874G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1004G>A
  hgvsp: ENSP00000414678.3:p.Arg335His
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*215G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1991G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1103G>A
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg289His
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-80442722-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442722
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442722
    reference: chr 17
allele count: 10709
allele frequency: 8.923423048079326e-2
allele num: 120010
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*216T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.690T>C
  hgvsp: ENST00000390006.4:c.690T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1005T>C
  hgvsp: ENST00000457415.3:c.1005T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.39T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*397T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1875T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.732T>C
  hgvsp: ENST00000577432.1:c.732T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.867T>C
  hgvsp: ENST00000309794.11:c.867T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.723T>C
  hgvsp: ENST00000345415.7:c.723T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1104T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.308T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-651T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1992T>C
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 7.75e1
  variant carriers: 613
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 8.75e1
  variant carriers: 575
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 9.75e1
  variant carriers: 4346
genotype depth: GenotypeDepth
  all individuals: 3632
  bin: 5.75e1
  variant carriers: 286
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 2.75e1
  variant carriers: 209
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 6.25e1
  variant carriers: 402
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 7072
  bin: 3.75e1
  variant carriers: 170
genotype depth: GenotypeDepth
  all individuals: 7252
  bin: 4.25e1
  variant carriers: 157
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4250
  bin: 2.25e1
  variant carriers: 177
genotype depth: GenotypeDepth
  all individuals: 6122
  bin: 3.25e1
  variant carriers: 217
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 4.75e1
  variant carriers: 162
genotype quality: GenotypeQuality
hgvs: p.Arg289Arg
num of homozygotes: 934
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

17-80442725-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442725
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442725
    reference: chr 17
allele count: 1
allele frequency: 8.320713584396998e-6
allele num: 120182
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1008T>C
  hgvsp: ENST00000457415.3:c.1008T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*400T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.735T>C
  hgvsp: ENST00000577432.1:c.735T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*219T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.693T>C
  hgvsp: ENST00000390006.4:c.693T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.42T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1878T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1995T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.726T>C
  hgvsp: ENST00000345415.7:c.726T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.870T>C
  hgvsp: ENST00000309794.11:c.870T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-648T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1107T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.311T>C
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5639
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7287
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His290His
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

17-80442727-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442727
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442727
    reference: chr 17
allele count: 2
allele frequency: 1.662952738883161e-5
allele num: 120268
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.872A>G
  hgvsp: ENSP00000309899.10:p.Asp291Gly
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*221A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.737A>G
  hgvsp: ENSP00000462792.1:p.Asp246Gly
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-646A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.1997A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.313A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.695A>G
  hgvsp: ENSP00000374656.4:p.Asp232Gly
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.44A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*402A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.728A>G
  hgvsp: ENSP00000283996.9:p.Asp243Gly
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1010A>G
  hgvsp: ENSP00000414678.3:p.Asp337Gly
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1109A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1880A>G
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7287
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp291Gly
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

17-80442733-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442733
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442733
    reference: chr 17
allele count: 1
allele frequency: 8.302751531857658e-6
allele num: 120442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1886C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.701C>T
  hgvsp: ENSP00000374656.4:p.Ala234Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1115C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.50C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*408C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.743C>T
  hgvsp: ENSP00000462792.1:p.Ala248Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-640C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2003C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1016C>T
  hgvsp: ENSP00000414678.3:p.Ala339Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.319C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.734C>T
  hgvsp: ENSP00000283996.9:p.Ala245Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.878C>T
  hgvsp: ENSP00000309899.10:p.Ala293Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*227C>T
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala293Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

17-80442743-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442743
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442743
    reference: chr 17
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.329C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*418C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1125C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-630C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.60C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1896C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.753C>T
  hgvsp: ENST00000577432.1:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1026C>T
  hgvsp: ENST00000457415.3:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*237C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.888C>T
  hgvsp: ENST00000309794.11:c.888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.744C>T
  hgvsp: ENST00000345415.7:c.744C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.711C>T
  hgvsp: ENST00000390006.4:c.711C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2013C>T
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5640
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp296Asp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-80442744-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442744
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442744
    reference: chr 17
allele count: 2
allele frequency: 1.656753756689143e-5
allele num: 120718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.712G>A
  hgvsp: ENSP00000374656.4:p.Gly238Arg
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2014G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-629G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1897G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1027G>A
  hgvsp: ENSP00000414678.3:p.Gly343Arg
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.745G>A
  hgvsp: ENSP00000283996.9:p.Gly249Arg
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.61G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.754G>A
  hgvsp: ENSP00000462792.1:p.Gly252Arg
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.889G>A
  hgvsp: ENSP00000309899.10:p.Gly297Arg
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*419G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.330G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1126G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*238G>A
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5640
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly297Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

17-80442753-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442753
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442753
    reference: chr 17
allele count: 1
allele frequency: 8.28225940036442e-6
allele num: 120740
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.721G>T
  hgvsp: ENSP00000374656.4:p.Ala241Ser
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2023G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1036G>T
  hgvsp: ENSP00000414678.3:p.Ala346Ser
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.763G>T
  hgvsp: ENSP00000462792.1:p.Ala255Ser
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.70G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.754G>T
  hgvsp: ENSP00000283996.9:p.Ala252Ser
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*428G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.898G>T
  hgvsp: ENSP00000309899.10:p.Ala300Ser
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*247G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1135G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.339G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1906G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-620G>T
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5686
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala300Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum

17-80442754-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442754
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442754
    reference: chr 17
allele count: 1
allele frequency: 8.283082632032337e-6
allele num: 120728
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1037C>T
  hgvsp: ENSP00000414678.3:p.Ala346Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1907C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-619C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.722C>T
  hgvsp: ENSP00000374656.4:p.Ala241Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.340C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.755C>T
  hgvsp: ENSP00000283996.9:p.Ala252Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.764C>T
  hgvsp: ENSP00000462792.1:p.Ala255Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.899C>T
  hgvsp: ENSP00000309899.10:p.Ala300Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*248C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1136C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2024C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*429C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.71C>T
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala300Val
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

17-80442757-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442757
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442757
    reference: chr 17
allele count: 1
allele frequency: 8.284043275842073e-6
allele num: 120714
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.902A>G
  hgvsp: ENSP00000309899.10:p.His301Arg
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.758A>G
  hgvsp: ENSP00000283996.9:p.His253Arg
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1139A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.767A>G
  hgvsp: ENSP00000462792.1:p.His256Arg
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*251A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*432A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1040A>G
  hgvsp: ENSP00000414678.3:p.His347Arg
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.725A>G
  hgvsp: ENSP00000374656.4:p.His242Arg
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.343A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.74A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1910A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-616A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2027A>G
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His301Arg
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum

17-80442759-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442759
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442759
    reference: chr 17
allele count: 19
allele frequency: 1.573889993373095e-4
allele num: 120720
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*253A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1141A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.727A>G
  hgvsp: ENSP00000374656.4:p.Ile243Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.904A>G
  hgvsp: ENSP00000309899.10:p.Ile302Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*434A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-614A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2029A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1042A>G
  hgvsp: ENSP00000414678.3:p.Ile348Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.760A>G
  hgvsp: ENSP00000283996.9:p.Ile254Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1912A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.345A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.76A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.769A>G
  hgvsp: ENSP00000462792.1:p.Ile257Val
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4649
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8118
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Ile302Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-80442767-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442767
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442767
    reference: chr 17
allele count: 1
allele frequency: 8.289949265510494e-6
allele num: 120628
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*442A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.912A>G
  hgvsp: ENST00000309794.11:c.912A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-606A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1149A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.353A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*261A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1920A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1050A>G
  hgvsp: ENST00000457415.3:c.1050A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.735A>G
  hgvsp: ENST00000390006.4:c.735A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.768A>G
  hgvsp: ENST00000345415.7:c.768A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.777A>G
  hgvsp: ENST00000577432.1:c.777A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.84A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2037A>G
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7114
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg304Arg
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

17-80442772-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442772
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442772
    reference: chr 17
allele count: 1
allele frequency: 8.296414289743973e-6
allele num: 120534
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*266C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.917C>G
  hgvsp: ENSP00000309899.10:p.Ala306Gly
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.740C>G
  hgvsp: ENSP00000374656.4:p.Ala247Gly
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.782C>G
  hgvsp: ENSP00000462792.1:p.Ala261Gly
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-601C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.773C>G
  hgvsp: ENSP00000283996.9:p.Ala258Gly
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1154C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.358C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1925C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1055C>G
  hgvsp: ENSP00000414678.3:p.Ala352Gly
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*447C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2042C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.89C>G
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala306Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

17-80442772-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442772
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442772
    reference: chr 17
allele count: 6
allele frequency: 4.977848573846384e-5
allele num: 120534
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.740C>T
  hgvsp: ENSP00000374656.4:p.Ala247Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.917C>T
  hgvsp: ENSP00000309899.10:p.Ala306Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-601C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2042C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1055C>T
  hgvsp: ENSP00000414678.3:p.Ala352Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.773C>T
  hgvsp: ENSP00000283996.9:p.Ala258Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.358C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*447C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.89C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.782C>T
  hgvsp: ENSP00000462792.1:p.Ala261Val
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*266C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1154C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1925C>T
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8294
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala306Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

17-80442773-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442773
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442773
    reference: chr 17
allele count: 5
allele frequency: 4.148207144871987e-5
allele num: 120534
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462792
  ensembl transcript: ENST00000577432
  gene symbol: NARF
  hgvsc: ENST00000577432.1:c.783G>A
  hgvsp: ENST00000577432.1:c.783G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1056G>A
  hgvsp: ENST00000457415.3:c.1056G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*448G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.741G>A
  hgvsp: ENST00000390006.4:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1926G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.359G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-600G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1155G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.774G>A
  hgvsp: ENST00000345415.7:c.774G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.90G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.918G>A
  hgvsp: ENST00000309794.11:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2043G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*267G>A
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8293
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala306Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

17-80442785-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442785
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442785
    reference: chr 17
allele count: 1
allele frequency: 8.339031671642289e-6
allele num: 119918
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.102G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.930G>A
  hgvsp: ENST00000309794.11:c.930G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1167G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1068G>A
  hgvsp: ENST00000457415.3:c.1068G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*460G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*279G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.753G>A
  hgvsp: ENST00000390006.4:c.753G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.786G>A
  hgvsp: ENST00000345415.7:c.786G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.371G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1938G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2055G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-588G>A
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu310Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

17-80442785-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442785
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442785
    reference: chr 17
allele count: 1
allele frequency: 8.339031671642289e-6
allele num: 119918
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1938G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.786G>C
  hgvsp: ENST00000345415.7:c.786G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*279G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-588G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*460G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.930G>C
  hgvsp: ENST00000309794.11:c.930G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.753G>C
  hgvsp: ENST00000390006.4:c.753G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.371G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1068G>C
  hgvsp: ENST00000457415.3:c.1068G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1167G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.102G>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2055G>C
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu310Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD

17-80442790-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442790
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442790
    reference: chr 17
allele count: 2
allele frequency: 1.67123470820242e-5
allele num: 119672
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.791A>G
  hgvsp: ENSP00000283996.9:p.Asn264Ser
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.935A>G
  hgvsp: ENSP00000309899.10:p.Asn312Ser
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1073A>G
  hgvsp: ENSP00000414678.3:p.Asn358Ser
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*284A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2060A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.758A>G
  hgvsp: ENSP00000374656.4:p.Asn253Ser
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1172A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1943A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*465A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.376A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-583A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.107A>G
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn312Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

17-80442791-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442791
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442791
    reference: chr 17
allele count: 2
allele frequency: 1.672464543751672e-5
allele num: 119584
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.108C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*466C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.792C>G
  hgvsp: ENSP00000283996.9:p.Asn264Lys
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-582C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*285C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1944C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1074C>G
  hgvsp: ENSP00000414678.3:p.Asn358Lys
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.936C>G
  hgvsp: ENSP00000309899.10:p.Asn312Lys
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.377C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.759C>G
  hgvsp: ENSP00000374656.4:p.Asn253Lys
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2061C>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1173C>G
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn312Lys
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

17-80442791-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442791
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442791
    reference: chr 17
allele count: 2
allele frequency: 1.672464543751672e-5
allele num: 119584
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.377C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.936C>T
  hgvsp: ENST00000309794.11:c.936C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*466C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-582C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1074C>T
  hgvsp: ENST00000457415.3:c.1074C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1173C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2061C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*285C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.759C>T
  hgvsp: ENST00000390006.4:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.108C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.792C>T
  hgvsp: ENST00000345415.7:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1944C>T
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn312Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

17-80442792-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442792
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442792
    reference: chr 17
allele count: 1
allele frequency: 8.37885846432282e-6
allele num: 119348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.793G>A
  hgvsp: ENSP00000283996.9:p.Glu265Lys
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.937G>A
  hgvsp: ENSP00000309899.10:p.Glu313Lys
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.109G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*286G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.760G>A
  hgvsp: ENSP00000374656.4:p.Glu254Lys
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1075G>A
  hgvsp: ENSP00000414678.3:p.Glu359Lys
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1174G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1945G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2062G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.378G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*467G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-581G>A
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7062
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu313Lys
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

17-80442801-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442801
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442801
    reference: chr 17
allele count: 1
allele frequency: 8.411419342899921e-6
allele num: 118886
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1084G>A
  hgvsp: ENSP00000414678.3:p.Glu362Lys
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*476G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*295G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1954G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.387G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.946G>A
  hgvsp: ENSP00000309899.10:p.Glu316Lys
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-572G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.802G>A
  hgvsp: ENSP00000283996.9:p.Glu268Lys
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.769G>A
  hgvsp: ENSP00000374656.4:p.Glu257Lys
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.118G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1183G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2071G>A
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu316Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD

17-80442815-C-CTG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442815
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442817
    reference: chr 17
allele count: 1
allele frequency: 8.523550570225534e-6
allele num: 117322
alternate allele: CTG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.816_817insTG
  hgvsp: ENSP00000283996.9:p.Arg273CysfsTer4
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*490_*491insTG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*309_*310insTG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-558_196-557insTG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1098_1099insTG
  hgvsp: ENSP00000414678.3:p.Arg367CysfsTer4
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.783_784insTG
  hgvsp: ENSP00000374656.4:p.Arg262CysfsTer4
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1968_1969insTG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.392+9_392+10insTG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2085_2086insTG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.123+9_123+10insTG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.960_961insTG
  hgvsp: ENSP00000309899.10:p.Arg321CysfsTer4
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1197_240+1198insTG
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg321CysfsTer4
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

17-80442816-CGAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442816
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442813
    reference: chr 17
allele count: 1
allele frequency: 8.535919147773831e-6
allele num: 117152
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*492_*494delGAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.392+11_392+13delGAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2087_2089delGAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-556_196-554delGAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*311_*313delGAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.962_964delGAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.785_787delGAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1100_1102delGAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.818_820delGAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1199_240+1201delGAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1970_1972delGAG
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.123+11_123+13delGAG
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg321_Ala322delinsPro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: CGAG
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

17-80442817-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442817
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442817
    reference: chr 17
allele count: 1
allele frequency: 8.547592997811816e-6
allele num: 116992
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.392+11G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*311G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1100G>A
  hgvsp: ENSP00000414678.3:p.Arg367Gln
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1199G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*492G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.962G>A
  hgvsp: ENSP00000309899.10:p.Arg321Gln
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-556G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.785G>A
  hgvsp: ENSP00000374656.4:p.Arg262Gln
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.818G>A
  hgvsp: ENSP00000283996.9:p.Arg273Gln
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2087G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1970G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.123+11G>A
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8289
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg321Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

17-80442821-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442821
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442821
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 116666
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1104C>T
  hgvsp: ENST00000457415.3:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2091C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.392+15C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.966C>T
  hgvsp: ENST00000309794.11:c.966C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.822C>T
  hgvsp: ENST00000345415.7:c.822C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.123+15C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*496C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1203C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.789C>T
  hgvsp: ENST00000390006.4:c.789C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*315C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-552C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1974C>T
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8288
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala322Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ

17-80442828-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442828
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442828
    reference: chr 17
allele count: 1
allele frequency: 8.622622311897494e-6
allele num: 115974
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1109+2T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2096+2T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.392+22T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.971+2T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-545T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.794+2T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*501+2T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*320+2T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.827+2T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1979+2T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.123+22T>C
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1210T>C
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: splice donor
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.971+2T>C
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

17-80442837-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442837
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442837
    reference: chr 17
allele count: 1
allele frequency: 8.689305203155955e-6
allele num: 115084
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.827+11G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.971+11G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.392+31G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.123+31G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.794+11G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-536G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1219G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2096+11G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1979+11G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1109+11G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*320+11G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*501+11G>T
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8002
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4028
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

17-80442842-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442842
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442842
    reference: chr 17
allele count: 1
allele frequency: 8.705947903607744e-6
allele num: 114864
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*501+16C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.971+16C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1979+16C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.123+36C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.827+16C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.392+36C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*320+16C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1224C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2096+16C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.794+16C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-531C>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1109+16C>T
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

17-80442845-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442845
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442845
    reference: chr 17
allele count: 1
allele frequency: 8.712774670221478e-6
allele num: 114774
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1227A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*501+19A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.794+19A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.392+39A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*320+19A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.123+39A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1109+19A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-528A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1979+19A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.827+19A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.971+19A>G
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2096+19A>G
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

17-80442846-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442846
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442846
    reference: chr 17
allele count: 4
allele frequency: 3.504591014228639e-5
allele num: 114136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-527G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.971+20G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1228G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.392+40G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1979+20G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*320+20G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.794+20G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.123+40G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*501+20G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2096+20G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1109+20G>A
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.827+20G>A
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4028
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7251
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

17-80442856-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 80442856
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 80442856
    reference: chr 17
allele count: 1
allele frequency: 8.792445530799936e-6
allele num: 113734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584965
  gene symbol: NARF
  hgvsc: ENST00000584965.1:n.240+1238G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462006
  ensembl transcript: ENST00000582907
  gene symbol: NARF
  hgvsc: ENST00000582907.1:c.*501+30G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000309899
  ensembl transcript: ENST00000309794
  gene symbol: NARF
  hgvsc: ENST00000309794.11:c.971+30G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000584445
  gene symbol: NARF
  hgvsc: ENST00000584445.1:n.1979+30G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000583908
  gene symbol: NARF
  hgvsc: ENST00000583908.1:n.392+50G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000578820
  gene symbol: NARF
  hgvsc: ENST00000578820.1:n.123+50G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000363739
  ensembl transcript: ENST00000374611
  gene symbol: NARF
  hgvsc: ENST00000374611.5:c.*320+30G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000462970
  ensembl transcript: ENST00000584513
  gene symbol: NARF
  hgvsc: ENST00000584513.1:c.196-517G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl transcript: ENST00000577812
  gene symbol: NARF
  hgvsc: ENST00000577812.1:n.2096+30G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000374656
  ensembl transcript: ENST00000390006
  gene symbol: NARF
  hgvsc: ENST00000390006.4:c.794+30G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000283996
  ensembl transcript: ENST00000345415
  gene symbol: NARF
  hgvsc: ENST00000345415.7:c.827+30G>T
  variant of: http://identifiers.org/hgnc/29916
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141562
  ensembl protein: ENSP00000414678
  ensembl transcript: ENST00000457415
  gene symbol: NARF
  hgvsc: ENST00000457415.3:c.1109+30G>T
  variant of: http://identifiers.org/hgnc/29916
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS

GenotypeDepth
all individuals: 425
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 101
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3976
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3199
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19125
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2168
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10804
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 188
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4609
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9495
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5614
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505978735580254e-5
allele num: 66402
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

DP
type: SiteQuality
SIO_000300: 2.049781e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

VQSLOD
type: SiteQuality
SIO_000300: 2.49e0

QD
type: SiteQuality
SIO_000300: 5.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.03e-1

GenotypeDepth
all individuals: 446
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3332
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 851
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 15802
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3187
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9282
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10793
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4586
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5583
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3942
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18496
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 5
allele frequency: 4.335009537020982e-4
allele num: 11534
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66340
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.318e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.038625e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e0

MQRankSum
type: SiteQuality
SIO_000300: 4.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

FS
type: SiteQuality
SIO_000300: 2.797e0

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

GenotypeDepth
all individuals: 261
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 446
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 253
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1787
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9336
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 111
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9257
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 399
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18270
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5575
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 4.52420449404313e-5
allele num: 66310
num of homozygotes: 0

BaseQRankSum
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SIO_000300: -2.776e0

FS
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MQ
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QD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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ClippingRankSum
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SIO_000300: 3.04e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.019961948479449e-5
allele num: 66226
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

ClippingRankSum
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SIO_000300: -2.18e-1

FS
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InbreedingCoeff
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MQ
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DP
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ReadPosRankSum
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MQRankSum
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QD
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BaseQRankSum
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SIO_000300: -1.46e-1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

Latino
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allele count: 11
allele frequency: 9.550269143948603e-4
allele num: 11518
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66218
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.315e0

DP
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SIO_000300: 2.031901e6

MQRankSum
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SIO_000300: -1.4e-1

QD
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ClippingRankSum
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FS
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ReadPosRankSum
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MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: 2.9e-3

VQSLOD
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SIO_000300: 1.47e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66294
num of homozygotes: 0

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

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

Latino
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allele count: 1
allele frequency: 8.676036786395974e-5
allele num: 11526
num of homozygotes: 0

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

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

MQ
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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DP
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QD
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SIO_000300: 1.187e1

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

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele num: 6602
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African
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Latino
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num of homozygotes: 0

QD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQ
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ReadPosRankSum
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

East Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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Other
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.042e0

FS
type: SiteQuality
SIO_000300: 8.577999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: -2.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.076e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

DP
type: SiteQuality
SIO_000300: 2.019729e6

VQSLOD
type: SiteQuality
SIO_000300: -1.734e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.442e0

GenotypeDepth
all individuals: 14482
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variant carriers: 0

GenotypeDepth
all individuals: 101
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 84
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variant carriers: 0

GenotypeDepth
all individuals: 1775
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1317
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2138
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10727
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 8680
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.430428970713331e-4
allele num: 16458
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66236
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.96e-2

FS
type: SiteQuality
SIO_000300: 7.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.0e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.38e-1

DP
type: SiteQuality
SIO_000300: 1.99933e6

QD
type: SiteQuality
SIO_000300: 1.605e1

GenotypeDepth
all individuals: 110
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variant carriers: 0

GenotypeDepth
all individuals: 6922
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 423
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GenotypeQuality
all individuals: 5215
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variant carriers: 0

GenotypeQuality
all individuals: 12574
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
all individuals: 7529
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2101
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3533
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.798157946306095e-5
allele num: 10206
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66010
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

MQRankSum
type: SiteQuality
SIO_000300: -8.139999999999999e-1

FS
type: SiteQuality
SIO_000300: 6.396e0

VQSLOD
type: SiteQuality
SIO_000300: -1.128e-1

DP
type: SiteQuality
SIO_000300: 1.947489e6

QD
type: SiteQuality
SIO_000300: 6.96e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.58e-1

GenotypeDepth
all individuals: 56
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5622
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1764
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variant carriers: 0

GenotypeQuality
all individuals: 3117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 127
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variant carriers: 0

GenotypeQuality
all individuals: 1354
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7529
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variant carriers: 0

GenotypeQuality
all individuals: 2122
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variant carriers: 0

GenotypeQuality
all individuals: 1689
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variant carriers: 0

GenotypeQuality
all individuals: 911
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variant carriers: 0

GenotypeQuality
all individuals: 1311
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 116
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2101
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12574
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variant carriers: 0

GenotypeQuality
all individuals: 1237
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10691
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 423
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variant carriers: 0

GenotypeQuality
all individuals: 3533
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4417
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5215
bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.709284096847239e-5
allele num: 11482
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514921981517952e-5
allele num: 66010
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.128e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

FS
type: SiteQuality
SIO_000300: 6.396e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 6.96e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e0

MQRankSum
type: SiteQuality
SIO_000300: -8.139999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-2

DP
type: SiteQuality
SIO_000300: 1.947489e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.58e-1

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

GenotypeDepth
all individuals: 8532
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 56
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variant carriers: 0

GenotypeDepth
all individuals: 451
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variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1306
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variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 2.75e1
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GenotypeQuality
all individuals: 1377
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variant carriers: 0

GenotypeQuality
all individuals: 52
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GenotypeQuality
all individuals: 1705
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variant carriers: 0

GenotypeQuality
all individuals: 108
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variant carriers: 0

GenotypeQuality
all individuals: 3116
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variant carriers: 0

GenotypeQuality
all individuals: 145
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variant carriers: 0

GenotypeQuality
all individuals: 3499
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variant carriers: 0

GenotypeQuality
all individuals: 7461
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variant carriers: 0

GenotypeQuality
all individuals: 4409
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variant carriers: 0

GenotypeQuality
all individuals: 2392
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variant carriers: 0

GenotypeQuality
all individuals: 1413
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variant carriers: 0

GenotypeQuality
all individuals: 5198
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variant carriers: 0

GenotypeQuality
all individuals: 12014
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variant carriers: 0

GenotypeQuality
all individuals: 2169
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GenotypeQuality
all individuals: 2103
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variant carriers: 0

GenotypeQuality
all individuals: 10687
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 480
bin: 5.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.742160278745645e-4
allele num: 11480
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.832841691248771e-5
allele num: 10170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.551937608108518e-5
allele num: 65906
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-2

DP
type: SiteQuality
SIO_000300: 1.941522e6

FS
type: SiteQuality
SIO_000300: 8.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.275e0

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.048e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

GenotypeDepth
all individuals: 6555
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2072
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1975
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3312
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 1

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1695
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variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 3.75e1
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GenotypeQuality
all individuals: 3547
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GenotypeQuality
all individuals: 628
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variant carriers: 0

GenotypeQuality
all individuals: 183
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GenotypeQuality
all individuals: 3873
bin: 6.25e1
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GenotypeQuality
all individuals: 3071
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
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GenotypeQuality
all individuals: 730
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34531
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2881
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.940357852882704e-5
allele num: 10060
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64396
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.979e1

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

QD
type: SiteQuality
SIO_000300: 1.355e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

FS
type: SiteQuality
SIO_000300: 2.327e0

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

DP
type: SiteQuality
SIO_000300: 2.691794e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.644e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e-1

GenotypeDepth
all individuals: 4091
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3873
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2072
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 628
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1975
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variant carriers: 0

GenotypeQuality
all individuals: 3547
bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 2881
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34531
bin: 9.75e1
variant carriers: 5

South Asian
type: Population
allele count: 2
allele frequency: 1.988071570576541e-4
allele num: 10060
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.949317738791423e-4
allele num: 10260
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.552891483943102e-5
allele num: 64396
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.691794e6

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

FS
type: SiteQuality
SIO_000300: 2.327e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

QD
type: SiteQuality
SIO_000300: 1.355e1

MQ
type: SiteQuality
SIO_000300: 5.979e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.644e0

GenotypeDepth
all individuals: 420
bin: 9.25e1
variant carriers: 16

GenotypeQuality
all individuals: 1007
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3900
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 34689
bin: 9.75e1
variant carriers: 570

GenotypeQuality
all individuals: 177
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 2.5e0
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GenotypeQuality
all individuals: 2306
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3287
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1686
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 591
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2884
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3522
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3039
bin: 7.75e1
variant carriers: 2

African
type: Population
allele count: 564
allele frequency: 5.497076023391813e-2
allele num: 10260
num of homozygotes: 18

Latino
type: Population
allele count: 20
allele frequency: 1.740341106856944e-3
allele num: 11492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 9.316191540898081e-5
allele num: 64404
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.164144353899884e-4
allele num: 8590
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.234567901234568e-3
allele num: 810
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

InbreedingCoeff
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SIO_000300: 3.79e-2

VQSLOD
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SIO_000300: 6.47e0

FS
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
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SIO_000300: 6.04e-1

DP
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SIO_000300: 2.697304e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e-1

BaseQRankSum
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SIO_000300: 2.87e0

QD
type: SiteQuality
SIO_000300: 1.351e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1697
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GenotypeQuality
all individuals: 3306
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 9.72951936174353e-5
allele num: 10278
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
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SIO_000300: 1.1e0

ReadPosRankSum
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SIO_000300: 7.15e-1

DP
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SIO_000300: 2.701618e6

ClippingRankSum
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FS
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SIO_000300: 0.0e0

MQ
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BaseQRankSum
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SIO_000300: -7.15e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.16e-1

QD
type: SiteQuality
SIO_000300: 8.130000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 410
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GenotypeQuality
all individuals: 34605
bin: 9.75e1
variant carriers: 15

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.319755033868423e-4
allele num: 64662
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10790
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.259e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.03e-1

InbreedingCoeff
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SIO_000300: 7.0e-4

ClippingRankSum
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SIO_000300: -1.73e-1

VQSLOD
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SIO_000300: 3.04e0

MQRankSum
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SIO_000300: 3.1e-1

DP
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SIO_000300: 2.70949e6

QD
type: SiteQuality
SIO_000300: 1.413e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
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SIO_000300: 3.25e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1999
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GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
all individuals: 1710
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10880
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545595054095827e-5
allele num: 64700
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.771e0

MQ
type: SiteQuality
SIO_000300: 6.041e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.354e0

DP
type: SiteQuality
SIO_000300: 2.710407e6

QD
type: SiteQuality
SIO_000300: 1.839e1

GenotypeDepth
all individuals: 2787
bin: 6.25e1
variant carriers: 249

GenotypeDepth
all individuals: 5409
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variant carriers: 161

GenotypeDepth
all individuals: 608
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variant carriers: 225

GenotypeQuality
all individuals: 3202
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variant carriers: 10

GenotypeQuality
all individuals: 75
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GenotypeQuality
all individuals: 2860
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variant carriers: 6

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
all individuals: 71
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variant carriers: 9

GenotypeQuality
all individuals: 3398
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
all individuals: 1920
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GenotypeQuality
all individuals: 2960
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
all individuals: 168
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variant carriers: 2

GenotypeQuality
all individuals: 37
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GenotypeQuality
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GenotypeQuality
all individuals: 29
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GenotypeQuality
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GenotypeQuality
all individuals: 1657
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
all individuals: 35835
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variant carriers: 3995

GenotypeQuality
all individuals: 2857
bin: 6.75e1
variant carriers: 7

African
type: Population
allele count: 610
allele frequency: 5.913144629701435e-2
allele num: 10316
num of homozygotes: 18

European (Non-Finnish)
type: Population
allele count: 1651
allele frequency: 2.539296810114122e-2
allele num: 65018
num of homozygotes: 20

Other
type: Population
allele count: 38
allele frequency: 4.513064133016627e-2
allele num: 842
num of homozygotes: 1

Latino
type: Population
allele count: 240
allele frequency: 2.084056964223689e-2
allele num: 11516
num of homozygotes: 2

South Asian
type: Population
allele count: 1218
allele frequency: 9.933126732996249e-2
allele num: 12262
num of homozygotes: 48

European (Finnish)
type: Population
allele count: 259
allele frequency: 3.915935893559117e-2
allele num: 6614
num of homozygotes: 4

East Asian
type: Population
allele count: 111
allele frequency: 1.286509040333797e-2
allele num: 8628
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.845844e6

BaseQRankSum
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SIO_000300: 3.1e0

ReadPosRankSum
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SIO_000300: 4.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.52e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.95e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 1.42e1

MQRankSum
type: SiteQuality
SIO_000300: 1.14e-1

GenotypeDepth
all individuals: 1313
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 1962
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GenotypeDepth
all individuals: 6949
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GenotypeQuality
all individuals: 3217
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 311
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GenotypeQuality
all individuals: 1929
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GenotypeQuality
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GenotypeQuality
all individuals: 2896
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 121
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GenotypeQuality
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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: 409
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GenotypeQuality
all individuals: 2966
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65060
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.31696014828545e-4
allele num: 8632
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.33e-1

InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.82e1

VQSLOD
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SIO_000300: -1.759e0

BaseQRankSum
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SIO_000300: -1.348e0

MQRankSum
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SIO_000300: -4.7e-2

QD
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SIO_000300: 1.09e1

DP
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SIO_000300: 2.839992e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.53e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4878
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variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.735809755250825e-4
allele num: 11522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65138
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12502
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 2.86e-1

BaseQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.86e1

ReadPosRankSum
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SIO_000300: 8.61e-1

ClippingRankSum
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SIO_000300: -1.96e-1

VQSLOD
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SIO_000300: -1.04e0

DP
type: SiteQuality
SIO_000300: 2.842068e6

GenotypeDepth
all individuals: 1072
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variant carriers: 0

GenotypeDepth
all individuals: 695
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variant carriers: 0

GenotypeDepth
all individuals: 582
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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
all individuals: 305
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GenotypeQuality
all individuals: 383
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GenotypeQuality
all individuals: 1931
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GenotypeQuality
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GenotypeQuality
all individuals: 62
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GenotypeQuality
all individuals: 3410
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GenotypeQuality
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GenotypeQuality
all individuals: 2894
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Finnish)
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East Asian
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European (Non-Finnish)
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African
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South Asian
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VQSLOD
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FS
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MQ
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InbreedingCoeff
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MQRankSum
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QD
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DP
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ReadPosRankSum
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 3.066449970868725e-5
allele num: 65222
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African
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East Asian
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South Asian
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Latino
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Other
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European (Finnish)
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QD
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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MQ
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FS
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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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num of homozygotes: 0

European (Non-Finnish)
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African
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South Asian
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East Asian
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European (Finnish)
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Other
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DP
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MQ
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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South Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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InbreedingCoeff
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MQ
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ClippingRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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FS
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 65582
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Other
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European (Finnish)
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South Asian
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Latino
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African
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East Asian
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VQSLOD
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BaseQRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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African
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South Asian
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East Asian
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European (Non-Finnish)
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InbreedingCoeff
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VQSLOD
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FS
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MQ
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ClippingRankSum
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ReadPosRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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South Asian
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African
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European (Non-Finnish)
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ClippingRankSum
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VQSLOD
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FS
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InbreedingCoeff
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MQRankSum
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MQ
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BaseQRankSum
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DP
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10

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: 10374
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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allele count: 9
allele frequency: 6.277901785714286e-4
allele num: 14336
num of homozygotes: 0

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

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

Latino
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num of homozygotes: 0

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

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

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

Other
type: Population
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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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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.536656181950157e-5
allele num: 66128
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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FS
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MQRankSum
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SIO_000300: 8.86e-1

BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQ
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VQSLOD
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DP
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SIO_000300: 2.880904e6

InbreedingCoeff
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SIO_000300: 2.0e-4

QD
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SIO_000300: 1.343e1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512218727316719e-5
allele num: 66128
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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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

Other
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allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: 9.51e-1

FS
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ClippingRankSum
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MQRankSum
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MQ
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BaseQRankSum
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DP
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SIO_000300: 2.880904e6

VQSLOD
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SIO_000300: 2.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
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SIO_000300: 1.343e1

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

African
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allele count: 1
allele frequency: 9.63020030816641e-5
allele num: 10384
num of homozygotes: 0

South Asian
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: 1.511395925276585e-5
allele num: 66164
num of homozygotes: 0

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

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

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

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

BaseQRankSum
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SIO_000300: -2.22e-1

MQRankSum
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SIO_000300: -1.03e-1

MQ
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SIO_000300: 5.958e1

DP
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VQSLOD
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SIO_000300: 2.15e0

InbreedingCoeff
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QD
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SIO_000300: 1.25e1

FS
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SIO_000300: 1.371e0

ClippingRankSum
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SIO_000300: -2.77e-1

ReadPosRankSum
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SIO_000300: -4.0e-3

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
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allele count: 1
allele frequency: 1.510300247689241e-5
allele num: 66212
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
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

Other
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allele count: 0
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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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
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SIO_000300: 2.883252e6

InbreedingCoeff
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FS
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QD
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ReadPosRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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SIO_000300: 5.895e1

BaseQRankSum
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SIO_000300: -1.194e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15434
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 27
allele frequency: 4.075840830867701e-4
allele num: 66244
num of homozygotes: 0

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

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

African
type: Population
allele count: 2
allele frequency: 1.92492781520693e-4
allele num: 10390
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: 5.86e-1

ClippingRankSum
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SIO_000300: -7.12e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
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QD
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SIO_000300: 1.334e1

DP
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MQRankSum
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SIO_000300: 3.02e-1

FS
type: SiteQuality
SIO_000300: 5.2e-1

InbreedingCoeff
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SIO_000300: -3.0e-4

ReadPosRankSum
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SIO_000300: 8.33e-1

GenotypeDepth
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variant carriers: 220

GenotypeDepth
all individuals: 1308
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variant carriers: 486

GenotypeDepth
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variant carriers: 588

GenotypeDepth
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variant carriers: 575

GenotypeDepth
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variant carriers: 472

GenotypeQuality
all individuals: 2826
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 43
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1612
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GenotypeQuality
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GenotypeQuality
all individuals: 7059
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GenotypeQuality
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variant carriers: 9708

GenotypeQuality
all individuals: 67
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GenotypeQuality
all individuals: 1821
bin: 8.75e1
variant carriers: 4

European (Finnish)
type: Population
allele count: 476
allele frequency: 7.19685515573027e-2
allele num: 6614
num of homozygotes: 15

African
type: Population
allele count: 3649
allele frequency: 3.512030798845043e-1
allele num: 10390
num of homozygotes: 657

South Asian
type: Population
allele count: 1689
allele frequency: 1.082831132196435e-1
allele num: 15598
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European (Non-Finnish)
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allele count: 3563
allele frequency: 5.373733108108108e-2
allele num: 66304
num of homozygotes: 105

East Asian
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allele frequency: 1.294797687861272e-2
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Latino
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allele frequency: 9.833938764919564e-2
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Other
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allele frequency: 9.304932735426009e-2
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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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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GenotypeDepth
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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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num of homozygotes: 0

Other
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European (Non-Finnish)
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European (Finnish)
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African
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Latino
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East Asian
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InbreedingCoeff
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DP
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QD
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ClippingRankSum
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MQ
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VQSLOD
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BaseQRankSum
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MQRankSum
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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 frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

Latino
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European (Non-Finnish)
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allele count: 1
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allele num: 66380
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South Asian
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European (Finnish)
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num of homozygotes: 0

East Asian
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Other
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MQRankSum
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BaseQRankSum
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FS
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MQ
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ClippingRankSum
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InbreedingCoeff
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DP
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VQSLOD
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 10394
num of homozygotes: 0

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

Latino
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.505615947484116e-5
allele num: 66418
num of homozygotes: 0

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

East Asian
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South Asian
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Other
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African
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Latino
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European (Non-Finnish)
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ClippingRankSum
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MQ
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DP
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QD
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InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66496
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East Asian
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Latino
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European (Finnish)
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African
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South Asian
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Other
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MQRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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FS
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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South Asian
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Latino
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African
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European (Non-Finnish)
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MQ
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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VQSLOD
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QD
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FS
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MQRankSum
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GenotypeDepth
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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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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

Other
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num of homozygotes: 0

South Asian
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allele frequency: 6.216585851050602e-5
allele num: 16086
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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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

European (Non-Finnish)
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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QD
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DP
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ReadPosRankSum
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FS
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MQ
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 19
allele frequency: 2.857314725697786e-4
allele num: 66496
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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Other
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VQSLOD
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BaseQRankSum
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DP
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MQRankSum
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MQ
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QD
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ClippingRankSum
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FS
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 896
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66468
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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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: 1

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66444
num of homozygotes: 0

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

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

African
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South Asian
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Other
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East Asian
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European (Non-Finnish)
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Latino
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ClippingRankSum
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QD
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FS
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3
allele frequency: 4.514808572116542e-5
allele num: 66448
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Other
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South Asian
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allele num: 15962
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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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VQSLOD
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QD
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SIO_000300: 1.452e1

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.35e-1

DP
type: SiteQuality
SIO_000300: 2.740023e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

MQ
type: SiteQuality
SIO_000300: 5.899e1

FS
type: SiteQuality
SIO_000300: 1.741e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-2

GenotypeDepth
all individuals: 3746
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1793
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3710
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508978421608571e-5
allele num: 66270
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15542
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.79e-1

QD
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SIO_000300: 1.447e1

InbreedingCoeff
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SIO_000300: 8.0e-4

ClippingRankSum
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SIO_000300: -6.19e-1

VQSLOD
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SIO_000300: 9.98e-1

FS
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SIO_000300: 4.13e0

MQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 2.730688e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508978421608571e-5
allele num: 66270
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15542
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.956e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.79e-1

FS
type: SiteQuality
SIO_000300: 4.13e0

DP
type: SiteQuality
SIO_000300: 2.730688e6

QD
type: SiteQuality
SIO_000300: 1.447e1

GenotypeDepth
all individuals: 783
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1913
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 2140
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66190
num of homozygotes: 0

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

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

East Asian
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allele count: 2
allele frequency: 2.312138728323699e-4
allele num: 8650
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15388
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 2.726047e6

FS
type: SiteQuality
SIO_000300: 4.948e0

ClippingRankSum
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SIO_000300: 2.86e-1

BaseQRankSum
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SIO_000300: 4.94e0

QD
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SIO_000300: 1.242e1

VQSLOD
type: SiteQuality
SIO_000300: 6.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-2

MQ
type: SiteQuality
SIO_000300: 5.953e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 187
bin: 2.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.022609116189094e-5
allele num: 66168
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15326
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.153e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 5.24e-1

DP
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VQSLOD
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ReadPosRankSum
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SIO_000300: 8.38e-1

BaseQRankSum
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InbreedingCoeff
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MQRankSum
type: SiteQuality
SIO_000300: -3.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3320
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7582
bin: 6.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.524859715516116e-5
allele num: 15326
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.511304558094547e-5
allele num: 66168
num of homozygotes: 0

VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQ
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DP
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 5.24e-1

QD
type: SiteQuality
SIO_000300: 1.153e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
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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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 frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.513042425709617e-5
allele num: 66092
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.018e0

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

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

GenotypeQuality
all individuals: 3376
bin: 6.75e1
variant carriers: 0

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

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

Other
type: Population
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African
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South Asian
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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 count: 1
allele frequency: 1.516208266367468e-5
allele num: 65954
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InbreedingCoeff
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MQRankSum
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FS
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DP
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ReadPosRankSum
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SIO_000300: 1.25e0

ClippingRankSum
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SIO_000300: -9.320000000000001e-1

VQSLOD
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MQ
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SIO_000300: 5.967e1

BaseQRankSum
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QD
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SIO_000300: 1.068e1

GenotypeDepth
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variant carriers: 0

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

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

East Asian
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allele frequency: 1.158211721102618e-4
allele num: 8634
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 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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65564
num of homozygotes: 0

VQSLOD
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SIO_000300: 2.15e0

ReadPosRankSum
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DP
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MQRankSum
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FS
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MQ
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BaseQRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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SIO_000300: 9.27e-1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65514
num of homozygotes: 0

Other
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 1.159017153453871e-4
allele num: 8628
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 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

FS
type: SiteQuality
SIO_000300: 8.43e-1

ClippingRankSum
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QD
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VQSLOD
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DP
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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SIO_000300: -2.28e-1

MQ
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SIO_000300: 5.886e1

GenotypeDepth
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variant carriers: 0

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

East 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 frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele num: 11528
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65408
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 frequency: 0.0e0
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num of homozygotes: 0

Other
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South Asian
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Latino
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num of homozygotes: 0

East Asian
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FS
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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DP
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QD
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MQ
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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: 6.75e1
variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

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

Other
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South Asian
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East Asian
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allele frequency: 1.160362032954282e-4
allele num: 8618
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Latino
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VQSLOD
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BaseQRankSum
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MQ
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InbreedingCoeff
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FS
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ClippingRankSum
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MQRankSum
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DP
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 836
num of homozygotes: 0

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

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

GenotypeQuality
all individuals: 32747
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 241
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3726
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1885
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3299
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3174
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3560
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2130
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3277
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.72951936174353e-5
allele num: 10278
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64940
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11990
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e-1

FS
type: SiteQuality
SIO_000300: 1.261e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.94e0

DP
type: SiteQuality
SIO_000300: 2.663133e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.73e-1

QD
type: SiteQuality
SIO_000300: 1.228e1

GenotypeDepth
all individuals: 2614
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2780
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3726
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32748
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 67
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1873
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3556
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1106
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3266
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3112
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2129
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4073
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64766
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.647920055775041e-4
allele num: 8606
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.973e1

QD
type: SiteQuality
SIO_000300: 1.423e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

FS
type: SiteQuality
SIO_000300: 5.321e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.189e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.75e-1

DP
type: SiteQuality
SIO_000300: 2.659656e6

GenotypeDepth
all individuals: 568
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3727
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 351
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 70
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3548
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2126
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1259
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32745
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4274
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1865
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3127
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2882
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.914244963451596e-5
allele num: 11218
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64704
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.65579e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.134e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

QD
type: SiteQuality
SIO_000300: 1.129e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.79e0

FS
type: SiteQuality
SIO_000300: 0.0e0