15-75130049-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130049
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130049
    reference: chr 15
allele count: 4
allele frequency: 9.091322332833311e-5
allele num: 43998
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1521+43C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1329+49C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1544+49C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.162+43C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*1003+43C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.200+49C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1213+49C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1136+49C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1368+43C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1335+43C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1452+43C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1757+43C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11487
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10185
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26554
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

15-75130060-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130060
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130060
    reference: chr 15
allele count: 1
allele frequency: 2.212585184529605e-5
allele num: 45196
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1452+32G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1368+32G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1335+32G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1757+32G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1521+32G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1329+38G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1136+38G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1213+38G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*1003+32G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1544+38G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.162+32G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.200+38G>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9210
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS

15-75130071-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130071
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130071
    reference: chr 15
allele count: 19
allele frequency: 4.029863408840248e-4
allele num: 47148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1213+27C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1452+21C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1521+21C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.200+27C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1136+27C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1335+21C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.162+21C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1329+27C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1544+27C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*1003+21C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1757+21C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1368+21C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 29709
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4945
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9669
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6885
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

15-75130071-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130071
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130071
    reference: chr 15
allele count: 1
allele frequency: 2.120980741494867e-5
allele num: 47148
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.200+27C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1452+21C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1544+27C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*1003+21C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1368+21C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1329+27C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1335+21C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1213+27C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1757+21C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1136+27C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.162+21C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1521+21C>G
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29709
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6885
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

15-75130072-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130072
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130072
    reference: chr 15
allele count: 1
allele frequency: 2.116491703352523e-5
allele num: 47248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*1003+20G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.200+26G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1329+26G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1452+20G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1368+20G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1335+20G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1136+26G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1521+20G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1213+26G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1544+26G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.162+20G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1757+20G>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6697
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29737
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9647
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

15-75130073-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130073
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130073
    reference: chr 15
allele count: 20
allele frequency: 4.189359028068705e-4
allele num: 47740
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1213+25C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1544+25C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*1003+19C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1368+19C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1452+19C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1329+25C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.162+19C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.200+25C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1335+19C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1521+19C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1136+25C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1757+19C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29899
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6367
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9573
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5277
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 1
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

15-75130075-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130075
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130075
    reference: chr 15
allele count: 1
allele frequency: 2.073656270736563e-5
allele num: 48224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1452+17C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1329+23C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1757+17C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1544+23C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.162+17C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*1003+17C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1335+17C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.200+23C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1368+17C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1521+17C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1213+23C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1136+23C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5535
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6010
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30060
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

15-75130077-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130077
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130077
    reference: chr 15
allele count: 3
allele frequency: 6.169792694965449e-5
allele num: 48624
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1757+15G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1368+15G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1521+15G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1213+21G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1544+21G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*1003+15G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1329+21G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1136+21G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1335+15G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.162+15G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1452+15G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.200+21G>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9542
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29968
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

15-75130079-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130079
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130079
    reference: chr 15
allele count: 1
allele frequency: 2.027163997567403e-5
allele num: 49330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1757+13G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1136+19G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1329+19G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1544+19G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1213+19G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1368+13G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.200+19G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*1003+13G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.162+13G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1452+13G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1521+13G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1335+13G>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9492
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29984
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-75130090-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130090
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130090
    reference: chr 15
allele count: 1
allele frequency: 1.898397752297061e-5
allele num: 52676
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1521+2T>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1757+2T>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.200+8T>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.162+2T>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1213+8T>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1452+2T>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1368+2T>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*1003+2T>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1335+2T>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1544+8T>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1329+8T>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1136+8T>G
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9668
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1335+2T>G
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

15-75130093-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130093
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130093
    reference: chr 15
allele count: 42439
allele frequency: 5.390037593984962e-1
allele num: 78736
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1520A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*1002A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1213+5A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1334A>G
  hgvsp: ENSP00000400312.2:p.Lys445Arg
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1367A>G
  hgvsp: ENSP00000457853.1:p.Lys456Arg
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1756A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.161A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1544+5A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1136+5A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1451A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.200+5A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1329+5A>G
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 6.25e1
  variant carriers: 681
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.75e1
  variant carriers: 583
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 2.75e1
  variant carriers: 1138
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.75e1
  variant carriers: 700
genotype depth: GenotypeDepth
  all individuals: 8572
  bin: 1.75e1
  variant carriers: 7927
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 3.25e1
  variant carriers: 589
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 3.75e1
  variant carriers: 542
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.75e1
  variant carriers: 396
genotype depth: GenotypeDepth
  all individuals: 16058
  bin: 1.25e1
  variant carriers: 12914
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 2.25e1
  variant carriers: 3075
genotype depth: GenotypeDepth
  all individuals: 16837
  bin: 7.5e0
  variant carriers: 8099
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 152
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.75e1
  variant carriers: 603
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 4.75e1
  variant carriers: 685
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 243
genotype quality: GenotypeQuality
hgvs: p.Lys445Arg
num of homozygotes: 10760
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

15-75130094-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130094
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130094
    reference: chr 15
allele count: 4
allele frequency: 6.160480517480364e-5
allele num: 64930
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.160A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1329+4A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1136+4A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1213+4A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.200+4A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*1001A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1519A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1450A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1333A>G
  hgvsp: ENSP00000400312.2:p.Lys445Glu
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1544+4A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1366A>G
  hgvsp: ENSP00000457853.1:p.Lys456Glu
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1755A>G
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24416
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13015
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys445Glu
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/15-75130098-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130098
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130098
    reference: chr 15
allele count: 1
allele frequency: 1.550243388211949e-5
allele num: 64506
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1213G>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1329G>T
  hgvsp: ENSP00000400312.2:p.Gln443His
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1362G>T
  hgvsp: ENSP00000457853.1:p.Gln454His
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1515G>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1751G>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1136G>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*997G>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1329G>T
  hgvsp: ENSP00000456051.1:p.Gln443His
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.156G>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1446G>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.200G>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1544G>T
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24596
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12877
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln443His
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

15-75130113-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130113
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130113
    reference: chr 15
allele count: 5
allele frequency: 7.946346269985061e-5
allele num: 62922
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*982A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1529A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1431A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1500A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1121A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1314A>G
  hgvsp: ENST00000569437.1:c.1314A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1347A>G
  hgvsp: ENST00000568667.1:c.1347A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1314A>G
  hgvsp: ENST00000440863.2:c.1314A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1198A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.141A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1736A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.185A>G
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24964
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13006
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6652
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu438Glu
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

15-75130121-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130121
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130121
    reference: chr 15
allele count: 3
allele frequency: 4.934210526315789e-5
allele num: 60800
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.133C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.177C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1190C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1339C>A
  hgvsp: ENST00000568667.1:c.1339C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1306C>A
  hgvsp: ENST00000440863.2:c.1306C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*974C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1306C>A
  hgvsp: ENST00000569437.1:c.1306C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1113C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1728C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1423C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1492C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1521C>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4370
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13413
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5782
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg436Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

15-75130130-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130130
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130130
    reference: chr 15
allele count: 2
allele frequency: 3.389256058295204e-5
allele num: 59010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1719C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1297C>A
  hgvsp: ENSP00000456051.1:p.Leu433Ile
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.168C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1512C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1181C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1330C>A
  hgvsp: ENSP00000457853.1:p.Leu444Ile
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1483C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1297C>A
  hgvsp: ENSP00000400312.2:p.Leu433Ile
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1104C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1414C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.124C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*965C>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13930
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5173
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu433Ile
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

15-75130131-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130131
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130131
    reference: chr 15
allele count: 1
allele frequency: 1.704448610874382e-5
allele num: 58670
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1482C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1296C>T
  hgvsp: ENST00000440863.2:c.1296C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1718C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.167C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1511C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1296C>T
  hgvsp: ENST00000569437.1:c.1296C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1329C>T
  hgvsp: ENST00000568667.1:c.1329C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*964C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.123C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1413C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1103C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1180C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13969
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn432Asn
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-75130133-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130133
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130133
    reference: chr 15
allele count: 1
allele frequency: 1.712622024319233e-5
allele num: 58390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1411A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1716A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1327A>G
  hgvsp: ENSP00000457853.1:p.Asn443Asp
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1178A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1294A>G
  hgvsp: ENSP00000400312.2:p.Asn432Asp
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1101A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.165A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1294A>G
  hgvsp: ENSP00000456051.1:p.Asn432Asp
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1509A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*962A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.121A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1480A>G
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14034
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25360
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn432Asp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

15-75130143-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130143
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130143
    reference: chr 15
allele count: 1
allele frequency: 1.795654516071108e-5
allele num: 55690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1474-4G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.115-4G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.155G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1321-4G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*956-4G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1710-4G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1172-4G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1095-4G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1288-4G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1405-4G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1288-4G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1503-4G>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14328
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7042
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25039
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1288-4G>A
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

15-75130150-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130150
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130150
    reference: chr 15
allele count: 1
allele frequency: 1.840197269147253e-5
allele num: 54342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.148T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1710-11T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1288-11T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1288-11T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.115-11T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1474-11T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1172-11T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1405-11T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1503-11T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*956-11T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1321-11T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1095-11T>C
  variant of: http://identifiers.org/hgnc/19703
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8449
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14648
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

15-75130156-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130156
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130156
    reference: chr 15
allele count: 1
allele frequency: 1.935583772065655e-5
allele num: 51664
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1405-17A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1503-17A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1321-17A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1172-17A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1474-17A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.115-17A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1095-17A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1288-17A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1288-17A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1710-17A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.142A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*956-17A>G
  variant of: http://identifiers.org/hgnc/19703
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14634
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10829
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

15-75130157-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130157
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130157
    reference: chr 15
allele count: 1
allele frequency: 1.938886303707151e-5
allele num: 51576
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.115-18C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1288-18C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1710-18C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1172-18C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1288-18C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1503-18C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.141C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1321-18C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1474-18C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1095-18C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1405-18C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*956-18C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14596
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10855
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  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: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

15-75130161-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130161
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130161
    reference: chr 15
allele count: 1
allele frequency: 1.983025303402872e-5
allele num: 50428
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.115-22A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.137A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1288-22A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1503-22A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1474-22A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1288-22A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1710-22A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1172-22A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1321-22A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1405-22A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*956-22A>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1095-22A>G
  variant of: http://identifiers.org/hgnc/19703
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11893
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22625
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP

15-75130165-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130165
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130165
    reference: chr 15
allele count: 1
allele frequency: 2.072968490878939e-5
allele num: 48240
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1172-26C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1710-26C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1474-26C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1095-26C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.133C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1288-26C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.115-26C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1503-26C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*956-26C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1321-26C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1405-26C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1288-26C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13831
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

15-75130169-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130169
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130169
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 42508
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.115-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1474-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1172-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1405-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1503-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1710-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1288-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1288-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.129C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1321-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1095-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*956-30C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16644
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20920
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

15-75130169-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130169
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130169
    reference: chr 15
allele count: 23
allele frequency: 5.410746212477651e-4
allele num: 42508
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1503-30C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1321-30C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1474-30C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1405-30C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.129C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1710-30C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1288-30C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1172-30C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1288-30C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1095-30C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.115-30C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*956-30C>G
  variant of: http://identifiers.org/hgnc/19703
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16644
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20920
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12270
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

15-75130173-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130173
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130173
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 38878
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1288-34C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.115-34C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1095-34C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1474-34C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1405-34C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1172-34C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1288-34C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.125C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*956-34C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1710-34C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1503-34C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1321-34C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21394
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17922
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ

15-75130177-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130177
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130177
    reference: chr 15
allele count: 2
allele frequency: 6.724949562878279e-5
allele num: 29740
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1288-38C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1288-38C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1710-38C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1405-38C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*956-38C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1474-38C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1321-38C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.115-38C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.121C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1095-38C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1503-38C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1172-38C>G
  variant of: http://identifiers.org/hgnc/19703
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7068
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23945
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18950
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

15-75130181-C-CG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130181
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130182
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 28052
alternate allele: CG
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1288-43dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1172-43dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.115-43dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*956-43dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.116dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1503-43dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1405-43dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1710-43dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1095-43dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1474-43dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1321-43dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1288-43dupC
  variant of: http://identifiers.org/hgnc/19703
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19309
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24311
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS

15-75130181-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130181
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130181
    reference: chr 15
allele count: 2
allele frequency: 7.129616426636246e-5
allele num: 28052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1405-42G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1288-42G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*956-42G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1172-42G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1474-42G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1288-42G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1321-42G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.115-42G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1503-42G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1095-42G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.117G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1710-42G>A
  variant of: http://identifiers.org/hgnc/19703
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19309
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24311
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6501
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum

15-75130182-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130182
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130182
    reference: chr 15
allele count: 1
allele frequency: 3.687859566307715e-5
allele num: 27116
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*956-43C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.116C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1095-43C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1288-43C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1503-43C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1288-43C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1321-43C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.115-43C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1710-43C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1474-43C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1405-43C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1172-43C>G
  variant of: http://identifiers.org/hgnc/19703
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19524
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24730
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

15-75130182-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130182
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130182
    reference: chr 15
allele count: 2
allele frequency: 7.375719132615431e-5
allele num: 27116
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1321-43C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1095-43C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.116C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1405-43C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1503-43C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1710-43C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1172-43C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1288-43C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1288-43C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1474-43C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*956-43C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.115-43C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24730
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5906
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19524
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

15-75130187-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130187
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130187
    reference: chr 15
allele count: 1
allele frequency: 3.821461326811372e-5
allele num: 26168
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1405-48C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.115-48C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1172-48C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1321-48C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1474-48C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1288-48C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1095-48C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*956-48C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1710-48C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.111C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1503-48C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1288-48C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25294
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19887
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: G
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

15-75130188-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130188
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130188
    reference: chr 15
allele count: 12
allele frequency: 5.046257359125315e-4
allele num: 23780
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1710-49A>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.115-49A>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1321-49A>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1288-49A>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.110A>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1405-49A>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1288-49A>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1095-49A>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1503-49A>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*956-49A>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1172-49A>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1474-49A>C
  variant of: http://identifiers.org/hgnc/19703
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25410
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19916
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

15-75130189-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130189
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130189
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 25854
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1288-50C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1503-50C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*956-50C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1288-50C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1405-50C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1474-50C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1172-50C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.115-50C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1710-50C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1321-50C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000568718
  gene symbol: ULK3
  hgvsc: ENST00000568718.1:n.109C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1095-50C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19889
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

15-75130462-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130462
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130463
    reference: chr 15
allele count: 1
allele frequency: 4.963271788763152e-5
allele num: 20148
alternate allele: GC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1287+30dupG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1502+30dupG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1171+30dupG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*955+30dupG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1473+30dupG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1320+30dupG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1287+30dupG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.114+30dupG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1709+30dupG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1404+30dupG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1094+30dupG
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35864
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP

15-75130462-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130462
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130461
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 20148
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1094+30delG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1709+30delG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1404+30delG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.114+30delG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1473+30delG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1287+30delG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1171+30delG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1287+30delG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*955+30delG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1502+30delG
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1320+30delG
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 8136
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35864
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: GC
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

15-75130465-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130465
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130465
    reference: chr 15
allele count: 1
allele frequency: 4.948535233570863e-5
allele num: 20208
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*955+28G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1094+28G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1404+28G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.114+28G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1473+28G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1320+28G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1287+28G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1502+28G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1709+28G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1287+28G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1171+28G>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35589
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1252
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

15-75130472-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130472
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130472
    reference: chr 15
allele count: 1
allele frequency: 4.91787154519524e-5
allele num: 20334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1320+21G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.114+21G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*955+21G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1171+21G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1709+21G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1287+21G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1502+21G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1473+21G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1287+21G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1404+21G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1094+21G>C
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10495
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34650
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1419
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

15-75130477-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130477
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130477
    reference: chr 15
allele count: 1
allele frequency: 4.892846658185733e-5
allele num: 20438
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.114+16G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1404+16G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*955+16G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1094+16G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1502+16G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1709+16G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1473+16G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1171+16G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1287+16G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1320+16G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1287+16G>C
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33755
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11896
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30897
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

15-75130488-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130488
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130488
    reference: chr 15
allele count: 1
allele frequency: 4.821135859608524e-5
allele num: 20742
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1473+5C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1287+5C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1502+5C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*955+5C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.114+5C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1171+5C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1094+5C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1709+5C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1320+5C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1287+5C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1404+5C>G
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1287+5C>G
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD

15-75130492-CCTCAGTGTGAAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130492
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130480
    reference: chr 15
allele count: 1
allele frequency: 4.772814051164567e-5
allele num: 20952
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsp: ENSP00000456051.1:p.Leu426_Glu429del
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsp: ENSP00000400312.2:p.Leu426_Glu429del
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsp: ENSP00000457853.1:p.Leu437_Glu440del
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30415
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu426_Glu429del
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: CCTCAGTGTGAAG
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

15-75130497-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130497
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130497
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 21124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1400C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1498C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1090C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.110C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1316C>T
  hgvsp: ENSP00000457853.1:p.Thr439Ile
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1283C>T
  hgvsp: ENSP00000400312.2:p.Thr428Ile
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1167C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1469C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1283C>T
  hgvsp: ENSP00000456051.1:p.Thr428Ile
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1705C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*951C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29320
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17551
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr428Ile
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

15-75130512-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130512
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130512
    reference: chr 15
allele count: 4
allele frequency: 1.834862385321101e-4
allele num: 21800
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1152G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1690G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1301G>A
  hgvsp: ENSP00000457853.1:p.Arg434Gln
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.95G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1075G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1483G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1268G>A
  hgvsp: ENSP00000456051.1:p.Arg423Gln
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1454G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*936G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1268G>A
  hgvsp: ENSP00000400312.2:p.Arg423Gln
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1385G>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2671
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25532
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21742
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg423Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

15-75130518-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130518
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130518
    reference: chr 15
allele count: 1
allele frequency: 4.505722267279445e-5
allele num: 22194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1069G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1379G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1146G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.89G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1452-4G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1262G>A
  hgvsp: ENSP00000456051.1:p.Arg421Gln
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1684G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1477G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1295G>A
  hgvsp: ENSP00000457853.1:p.Arg432Gln
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1262G>A
  hgvsp: ENSP00000400312.2:p.Arg421Gln
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*930G>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23877
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg421Gln
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-75130519-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130519
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130519
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 22314
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1452-5C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1261C>T
  hgvsp: ENSP00000456051.1:p.Arg421Trp
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1294C>T
  hgvsp: ENSP00000457853.1:p.Arg432Trp
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1145C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*929C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.88C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1683C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1261C>T
  hgvsp: ENSP00000400312.2:p.Arg421Trp
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1476C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1378C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1068C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 23674
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23636
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg421Trp
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

15-75130523-C-CG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130523
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130524
    reference: chr 15
allele count: 1
allele frequency: 4.437738528445904e-5
allele num: 22534
alternate allele: CG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1452-10dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1678dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.83dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1140dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*924dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1471dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1256dupC
  hgvsp: ENSP00000456051.1:p.Arg421ProfsTer9
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1373dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1289dupC
  hgvsp: ENSP00000457853.1:p.Arg432ProfsTer9
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1063dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1256dupC
  hgvsp: ENSP00000400312.2:p.Arg421ProfsTer9
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22999
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg421ProfsTer9
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

15-75130524-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130524
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130524
    reference: chr 15
allele count: 2
allele frequency: 8.816787162757891e-5
allele num: 22684
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1256C>T
  hgvsp: ENSP00000456051.1:p.Pro419Leu
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*924C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1256C>T
  hgvsp: ENSP00000400312.2:p.Pro419Leu
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1373C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1140C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1678C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1289C>T
  hgvsp: ENSP00000457853.1:p.Pro430Leu
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.83C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1063C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1452-10C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1471C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22647
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Pro419Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP

15-75130524-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130524
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130524
    reference: chr 15
allele count: 1
allele frequency: 4.408393581378945e-5
allele num: 22684
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1471C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1678C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.83C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*924C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1289C>G
  hgvsp: ENSP00000457853.1:p.Pro430Arg
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1063C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1256C>G
  hgvsp: ENSP00000456051.1:p.Pro419Arg
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1140C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1452-10C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1373C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1256C>G
  hgvsp: ENSP00000400312.2:p.Pro419Arg
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22647
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro419Arg
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-75130528-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130528
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130528
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 23058
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1674C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*920C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1452-14C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1369C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1136C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1252C>T
  hgvsp: ENSP00000456051.1:p.Pro418Ser
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1252C>T
  hgvsp: ENSP00000400312.2:p.Pro418Ser
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1285C>T
  hgvsp: ENSP00000457853.1:p.Pro429Ser
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1059C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.79C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1467C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25066
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22074
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro418Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP

15-75130532-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130532
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130532
    reference: chr 15
allele count: 1
allele frequency: 4.291845493562232e-5
allele num: 23300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1463G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1248G>A
  hgvsp: ENST00000440863.2:c.1248G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.75G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1248G>A
  hgvsp: ENST00000569437.1:c.1248G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1365G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1281G>A
  hgvsp: ENST00000568667.1:c.1281G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1670G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1132G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*916G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1452-18G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1055G>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21527
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25574
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1248G>A
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD

15-75130533-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130533
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130533
    reference: chr 15
allele count: 1
allele frequency: 4.283755997258396e-5
allele num: 23344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1280C>T
  hgvsp: ENSP00000457853.1:p.Ala427Val
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1247C>T
  hgvsp: ENSP00000400312.2:p.Ala416Val
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1247C>T
  hgvsp: ENSP00000456051.1:p.Ala416Val
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1462C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1452-19C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1054C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.74C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1131C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*915C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1364C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1669C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25710
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21331
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala416Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

15-75130563-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130563
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130563
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 24942
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.74-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1247-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1280-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1131-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1669-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1451+44C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*915-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1247-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1462-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1054-30C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1364-30C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19221
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19444
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

15-75130564-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130564
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130564
    reference: chr 15
allele count: 1
allele frequency: 4.000960230455309e-5
allele num: 24994
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1131-31C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1364-31C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.74-31C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1054-31C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1462-31C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1247-31C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1247-31C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*915-31C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1669-31C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1451+43C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1280-31C>G
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19230
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26511
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 2.5e0
  variant carriers: 0
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: G
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

15-75130569-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130569
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130569
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 25394
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1247-36G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1462-36G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.74-36G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1364-36G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1131-36G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1054-36G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1247-36G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1280-36G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*915-36G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1669-36G>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1451+38G>C
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18755
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26533
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS

15-75130569-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130569
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130569
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 25394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1054-36G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*915-36G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1364-36G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1462-36G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1669-36G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1247-36G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.74-36G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1280-36G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1247-36G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1131-36G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1451+38G>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 26533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18755
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

15-75130573-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130573
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130573
    reference: chr 15
allele count: 20748
allele frequency: 5.748323821133706e-1
allele num: 36094
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1364-40T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1246+34T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1130+34T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1053+34T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*914+34T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.74-40T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1451+34T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1461+34T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1668+34T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1279+34T>C
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1246+34T>C
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 2.25e1
  variant carriers: 592
genotype depth: GenotypeDepth
  all individuals: 24824
  bin: 7.5e0
  variant carriers: 15951
genotype depth: GenotypeDepth
  all individuals: 11666
  bin: 2.5e0
  variant carriers: 3665
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 7800
  bin: 1.25e1
  variant carriers: 6885
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 158
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 3.75e1
  variant carriers: 840
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.25e1
  variant carriers: 771
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.75e1
  variant carriers: 518
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 5.25e1
  variant carriers: 634
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 3.25e1
  variant carriers: 750
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 107
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 313
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 1.75e1
  variant carriers: 1444
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 2.75e1
  variant carriers: 695
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 4.75e1
  variant carriers: 770
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.75e1
  variant carriers: 430
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 243
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 4.75e1
  variant carriers: 595
num of homozygotes: 5567
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

15-75130578-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130578
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130578
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 27204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1246+29G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1364-45G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*914+29G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1668+29G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1461+29G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1279+29G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1451+29G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1053+29G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.74-45G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1246+29G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1130+29G>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22216
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21871
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

15-75130581-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130581
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130582
    reference: chr 15
allele count: 1
allele frequency: 3.744757339724386e-5
allele num: 26704
alternate allele: TG
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1246+25dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1246+25dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.74-49dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1451+25dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1364-49dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1461+25dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1668+25dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*914+25dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1130+25dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1053+25dupC
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1279+25dupC
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22683
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21740
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP

15-75130582-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130582
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130582
    reference: chr 15
allele count: 2
allele frequency: 7.49063670411985e-5
allele num: 26700
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*914+25C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1130+25C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1451+25C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1246+25C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1279+25C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.74-49C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1364-49C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1246+25C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1461+25C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1668+25C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1053+25C>G
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21646
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 22947
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

15-75130582-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130582
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130582
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 26700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1451+25C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.74-49C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*914+25C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1246+25C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1246+25C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1279+25C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1130+25C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1364-49C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1668+25C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1461+25C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1053+25C>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21646
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22947
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff

15-75130583-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130583
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130583
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 26616
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1246+24C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*914+24C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1364-50C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1246+24C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1668+24C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1053+24C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1451+24C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1130+24C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1461+24C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1279+24C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.74-50C>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23142
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21589
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1336
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD

15-75130585-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130585
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130585
    reference: chr 15
allele count: 7
allele frequency: 2.745313357910424e-4
allele num: 25498
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1364-52C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.74-52C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1053+22C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1279+22C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1461+22C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*914+22C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1130+22C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1668+22C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1246+22C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1451+22C>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1246+22C>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23846
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21165
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

15-75130586-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130586
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130586
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 25528
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.74-53C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1130+21C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1668+21C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*914+21C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1364-53C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1246+21C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1279+21C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1053+21C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1246+21C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1461+21C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1451+21C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23904
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21186
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3613
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

15-75130587-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130587
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130587
    reference: chr 15
allele count: 39
allele frequency: 1.534587235382073e-3
allele num: 25414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1461+20C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1668+20C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1246+20C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1053+20C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1451+20C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.74-54C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1246+20C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1130+20C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1279+20C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*914+20C>T
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1364-54C>T
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23906
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21236
  bin: 7.5e0
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS

15-75130587-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130587
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130587
    reference: chr 15
allele count: 1
allele frequency: 3.934839065082238e-5
allele num: 25414
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1451+20C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1246+20C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.74-54C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1279+20C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1130+20C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1668+20C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1461+20C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*914+20C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1053+20C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1246+20C>G
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1364-54C>G
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23906
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

15-75130600-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130600
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130600
    reference: chr 15
allele count: 7
allele frequency: 2.941423649046139e-4
allele num: 23798
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456051
  ensembl transcript: ENST00000569437
  gene symbol: ULK3
  hgvsc: ENST00000569437.1:c.1246+7G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000561725
  gene symbol: ULK3
  hgvsc: ENST00000561725.1:n.1461+7G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000455395
  ensembl transcript: ENST00000566631
  gene symbol: ULK3
  hgvsc: ENST00000566631.1:c.*914+7G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1451+7G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000454583
  ensembl transcript: ENST00000568273
  gene symbol: ULK3
  hgvsc: ENST00000568273.1:c.*1053+7G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000565881
  gene symbol: ULK3
  hgvsc: ENST00000565881.1:n.1364-67G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000567472
  gene symbol: ULK3
  hgvsc: ENST00000567472.1:n.74-67G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1246+7G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000457853
  ensembl transcript: ENST00000568667
  gene symbol: ULK3
  hgvsc: ENST00000568667.1:c.1279+7G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000570276
  gene symbol: ULK3
  hgvsc: ENST00000570276.1:n.1668+7G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000456296
  ensembl transcript: ENST00000568210
  gene symbol: ULK3
  hgvsc: ENST00000568210.1:c.*1130+7G>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20695
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1246+7G>A
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

15-75130604-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75130604
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 75130604
    reference: chr 15
allele count: 1
allele frequency: 4.23872499152255e-5
allele num: 23592
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl protein: ENSP00000400312
  ensembl transcript: ENST00000440863
  gene symbol: ULK3
  hgvsc: ENST00000440863.2:c.1246+3G>A
  variant of: http://identifiers.org/hgnc/19703
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140474
  ensembl transcript: ENST00000566479
  gene symbol: ULK3
  hgvsc: ENST00000566479.1:n.1451+3G>A
  variant of: http://identifiers.org/hgnc/19703
canonical: true
consequence: splice region
filter: PASS
hgvs: c.1246+3G>A
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 266
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 344
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4926
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8938
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19418
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2039
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5322
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3901
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3624
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2744
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2991
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1254
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4548
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3092
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9090
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 1.429592566118656e-3
allele num: 2798
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1262
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.95e-2

DP
type: SiteQuality
SIO_000300: 7.59651e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -2.682e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

FS
type: SiteQuality
SIO_000300: 8.023e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.87e-1

GenotypeDepth
all individuals: 205
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3863
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3656
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1770
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8044
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2931
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2635
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24945
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1336
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2751
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 477
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4280
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 372
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3270
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.250977724876721e-5
allele num: 23524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1328
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9164
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 1.155e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.07e0

DP
type: SiteQuality
SIO_000300: 7.9183e5

ClippingRankSum
type: SiteQuality
SIO_000300: 4.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.62e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.85e-2

FS
type: SiteQuality
SIO_000300: 2.434e0

GenotypeDepth
all individuals: 79
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 344
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1781
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5715
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 376
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27857
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 175
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1446
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 303
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3595
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6351
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3604
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 300
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1814
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2787
bin: 9.75e1
variant carriers: 20

GenotypeQuality
all individuals: 596
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 752
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 346
bin: 9.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3072
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 19
allele frequency: 7.694799935201685e-4
allele num: 24692
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4752
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9312
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1442
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.033e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.15e-1

FS
type: SiteQuality
SIO_000300: 2.813e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.28e-2

DP
type: SiteQuality
SIO_000300: 8.26638e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.39e-1

GenotypeDepth
all individuals: 9669
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 344
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27857
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5715
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1781
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1814
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6351
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3595
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3604
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2787
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 596
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24692
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4752
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.255208333333333e-4
allele num: 3072
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3496
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1442
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.28e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.033e1

FS
type: SiteQuality
SIO_000300: 2.813e0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.39e-1

DP
type: SiteQuality
SIO_000300: 8.26638e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

GenotypeDepth
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1489
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5736
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2768
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1442
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27897
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1893
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1743
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6207
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3596
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 345
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3557
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 320
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 2.099958000839983e-4
allele num: 4762
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24778
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3070
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1436
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.37e-2

QD
type: SiteQuality
SIO_000300: 1.086e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.06e-1

DP
type: SiteQuality
SIO_000300: 8.30451e5

GenotypeDepth
all individuals: 133
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3508
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28414
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3575
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 365
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 767
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6049
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1466
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 611
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2789
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 5925
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1467
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1634
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1480
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.06951871657754e-4
allele num: 9350
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.194888178913738e-4
allele num: 3130
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 8.347245409015025e-4
allele num: 4792
num of homozygotes: 0

East Asian
type: Population
allele count: 13
allele frequency: 3.653738055087128e-3
allele num: 3558
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.992015968063872e-5
allele num: 25050
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.35716e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.81e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.22e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.25e0

FS
type: SiteQuality
SIO_000300: 3.203e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

QD
type: SiteQuality
SIO_000300: 1.413e1

GenotypeDepth
all individuals: 79
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1856
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28692
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1490
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
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variant carriers: 0

GenotypeQuality
all individuals: 2778
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 373
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1480
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3552
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1573
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1442
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5630
bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 663
bin: 7.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.953819389530286e-5
allele num: 25292
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 8.41388e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

BaseQRankSum
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SIO_000300: -1.945e0

ReadPosRankSum
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SIO_000300: 2.2e0

FS
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QD
type: SiteQuality
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MQRankSum
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SIO_000300: -1.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.24e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.284e0

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
type: Population
allele count: 2
allele frequency: 5.524861878453039e-4
allele num: 3620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3218
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.90991554582421e-5
allele num: 25576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1540
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9424
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQRankSum
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SIO_000300: -2.77e-1

VQSLOD
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FS
type: SiteQuality
SIO_000300: 1.297e0

MQ
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DP
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SIO_000300: 8.46166e5

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

QD
type: SiteQuality
SIO_000300: 1.936e1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 364
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GenotypeQuality
all individuals: 1526
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.839950848629138e-5
allele num: 26042
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3670
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3300
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.52288e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.68e-1

VQSLOD
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SIO_000300: -7.08e-2

QD
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SIO_000300: 1.809e1

MQRankSum
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SIO_000300: 5.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.37e-1

InbreedingCoeff
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SIO_000300: -1.15e-2

FS
type: SiteQuality
SIO_000300: 1.443e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.11e-1

GenotypeDepth
all individuals: 93
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 963
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variant carriers: 0

GenotypeDepth
all individuals: 25
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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: 317
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GenotypeQuality
all individuals: 619
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5102
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4038
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.5650623885918e-5
allele num: 28050
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.667e0

QD
type: SiteQuality
SIO_000300: 1.406e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.900000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.246e0

FS
type: SiteQuality
SIO_000300: 3.09e0

VQSLOD
type: SiteQuality
SIO_000300: 3.2e-1

DP
type: SiteQuality
SIO_000300: 8.85583e5

GenotypeDepth
all individuals: 732
bin: 5.25e1
variant carriers: 711

GenotypeDepth
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variant carriers: 741

GenotypeDepth
all individuals: 317
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variant carriers: 317

GenotypeDepth
all individuals: 442
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variant carriers: 442

GenotypeDepth
all individuals: 775
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variant carriers: 562

GenotypeQuality
all individuals: 1248
bin: 5.25e1
variant carriers: 1088

GenotypeQuality
all individuals: 855
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variant carriers: 781

GenotypeQuality
all individuals: 2729
bin: 3.25e1
variant carriers: 2251

GenotypeQuality
all individuals: 2192
bin: 3.75e1
variant carriers: 1968

GenotypeQuality
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variant carriers: 593

GenotypeQuality
all individuals: 22647
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variant carriers: 22443

GenotypeQuality
all individuals: 1837
bin: 1.75e1
variant carriers: 1510

GenotypeQuality
all individuals: 1871
bin: 2.75e1
variant carriers: 1228

GenotypeQuality
all individuals: 4018
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variant carriers: 808

GenotypeQuality
all individuals: 1414
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variant carriers: 1313

GenotypeQuality
all individuals: 1034
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variant carriers: 937

GenotypeQuality
all individuals: 827
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variant carriers: 748

GenotypeQuality
all individuals: 805
bin: 1.25e1
variant carriers: 606

GenotypeQuality
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bin: 2.5e0
variant carriers: 200

GenotypeQuality
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variant carriers: 469

GenotypeQuality
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variant carriers: 2038

GenotypeQuality
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variant carriers: 373

GenotypeQuality
all individuals: 1261
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variant carriers: 644

GenotypeQuality
all individuals: 710
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variant carriers: 634

GenotypeQuality
all individuals: 711
bin: 7.75e1
variant carriers: 468

East Asian
type: Population
allele count: 2115
allele frequency: 3.825976845151954e-1
allele num: 5528
num of homozygotes: 309

Other
type: Population
allele count: 306
allele frequency: 5.3125e-1
allele num: 576
num of homozygotes: 73

South Asian
type: Population
allele count: 5983
allele frequency: 5.054917201757351e-1
allele num: 11836
num of homozygotes: 1448

European (Non-Finnish)
type: Population
allele count: 27667
allele frequency: 6.108854051667034e-1
allele num: 45290
num of homozygotes: 7709

Latino
type: Population
allele count: 3228
allele frequency: 5.065913370998116e-1
allele num: 6372
num of homozygotes: 628

African
type: Population
allele count: 1172
allele frequency: 2.020689655172414e-1
allele num: 5800
num of homozygotes: 93

European (Finnish)
type: Population
allele count: 1968
allele frequency: 5.902819436112777e-1
allele num: 3334
num of homozygotes: 500

VQSLOD
type: SiteQuality
SIO_000300: 5.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.88e-1

DP
type: SiteQuality
SIO_000300: 1.167818e6

MQRankSum
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SIO_000300: 1.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e-1

MQ
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SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.024e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.039e-1

FS
type: SiteQuality
SIO_000300: 5.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
all individuals: 2673
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 880
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4928
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.106561912138984e-4
allele num: 36148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4922
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e-2

MQ
type: SiteQuality
SIO_000300: 5.858e1

FS
type: SiteQuality
SIO_000300: 5.79e-1

MQRankSum
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 2.96e-1

InbreedingCoeff
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QD
type: SiteQuality
SIO_000300: 1.129e1

VQSLOD
type: SiteQuality
SIO_000300: -6.346000000000001e-1

DP
type: SiteQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 254
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4896
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.791424743188923e-5
allele num: 35824
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2312
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQ
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VQSLOD
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MQRankSum
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BaseQRankSum
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SIO_000300: -2.219e0

InbreedingCoeff
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SIO_000300: -8.6e-3

FS
type: SiteQuality
SIO_000300: 2.113e0

ClippingRankSum
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SIO_000300: -8.76e-1

DP
type: SiteQuality
SIO_000300: 8.59979e5

QD
type: SiteQuality
SIO_000300: 9.5e0

GenotypeDepth
all individuals: 21
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variant carriers: 0

GenotypeDepth
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 488
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GenotypeQuality
all individuals: 10558
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GenotypeQuality
all individuals: 262
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GenotypeQuality
all individuals: 142
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GenotypeQuality
all individuals: 394
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

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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

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

African
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allele frequency: 9.067827348567283e-4
allele num: 5514
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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allele frequency: 0.0e0
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East Asian
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num of homozygotes: 0

InbreedingCoeff
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DP
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VQSLOD
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QD
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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FS
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MQ
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ClippingRankSum
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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

East Asian
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allele frequency: 4.306632213608958e-4
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European (Non-Finnish)
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allele frequency: 2.997601918465228e-5
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num of homozygotes: 0

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

African
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DP
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SIO_000300: 8.3294e5

ClippingRankSum
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FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4274
num of homozygotes: 0

South Asian
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allele frequency: 1.951219512195122e-4
allele num: 10250
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East Asian
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African
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allele frequency: 0.0e0
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European (Finnish)
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Other
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num of homozygotes: 0

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

FS
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SIO_000300: 1.081e0

DP
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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MQ
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QD
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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: 1

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1970
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 1.901863826550019e-4
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 32084
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QD
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SIO_000300: 1.471e1

ClippingRankSum
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SIO_000300: -3.65e-1

MQ
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SIO_000300: 5.906e1

FS
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DP
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VQSLOD
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InbreedingCoeff
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SIO_000300: -1.23e-2

MQRankSum
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: 7.41e-1

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

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

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

South Asian
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allele num: 10222
num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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FS
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ReadPosRankSum
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InbreedingCoeff
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QD
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MQ
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MQRankSum
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VQSLOD
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DP
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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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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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African
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allele num: 5126
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Other
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European (Non-Finnish)
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European (Finnish)
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Latino
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allele frequency: 0.0e0
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ClippingRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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FS
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DP
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InbreedingCoeff
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QD
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MQRankSum
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BaseQRankSum
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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

African
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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: 3.410641200545703e-5
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European (Finnish)
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East Asian
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Other
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Latino
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 6.385696040868455e-4
allele num: 1566
num of homozygotes: 0

European (Non-Finnish)
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East Asian
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African
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num of homozygotes: 0

Latino
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Other
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South Asian
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InbreedingCoeff
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ClippingRankSum
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FS
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VQSLOD
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MQRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
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MQ
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DP
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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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Other
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South Asian
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European (Non-Finnish)
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East Asian
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European (Finnish)
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African
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Latino
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MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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BaseQRankSum
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FS
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MQRankSum
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QD
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VQSLOD
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ClippingRankSum
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DP
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ReadPosRankSum
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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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num of homozygotes: 0

South Asian
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Other
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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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MQ
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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QD
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DP
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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

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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European (Non-Finnish)
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allele count: 1
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allele num: 25496
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Other
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South Asian
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Latino
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East Asian
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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ClippingRankSum
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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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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1132
num of homozygotes: 0

European (Non-Finnish)
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South Asian
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African
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Latino
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Other
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East Asian
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ClippingRankSum
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QD
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BaseQRankSum
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FS
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MQRankSum
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 4230
num of homozygotes: 0

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

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

European (Non-Finnish)
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Other
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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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InbreedingCoeff
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VQSLOD
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QD
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ReadPosRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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DP
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MQRankSum
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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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bin: 1.25e1
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GenotypeQuality
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bin: 9.75e1
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.503401360544217e-4
allele num: 1176
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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allele frequency: 0.0e0
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African
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allele frequency: 3.190810465858328e-4
allele num: 3134
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 14030
num of homozygotes: 0

East Asian
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num of homozygotes: 0

FS
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SIO_000300: 0.0e0

DP
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ReadPosRankSum
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QD
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MQRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -2.25e-1

InbreedingCoeff
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SIO_000300: -4.1e-2

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

Other
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East Asian
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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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

European (Non-Finnish)
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num of homozygotes: 0

InbreedingCoeff
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DP
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ReadPosRankSum
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VQSLOD
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QD
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BaseQRankSum
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MQRankSum
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MQ
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ClippingRankSum
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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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GenotypeQuality
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variant carriers: 1

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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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

South Asian
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African
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allele num: 2948
num of homozygotes: 0

Latino
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East Asian
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BaseQRankSum
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SIO_000300: 9.56e-1

ReadPosRankSum
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FS
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ClippingRankSum
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MQ
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QD
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DP
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InbreedingCoeff
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VQSLOD
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MQRankSum
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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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2814
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 1.204819277108434e-4
allele num: 8300
num of homozygotes: 0

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

East Asian
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allele count: 0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 0.0e0

FS
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SIO_000300: 1.1129e1

MQ
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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DP
type: SiteQuality
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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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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2814
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 12582
num of homozygotes: 0

Other
type: Population
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allele frequency: 3.90625e-3
allele num: 256
num of homozygotes: 0

Latino
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South Asian
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allele num: 8300
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European (Finnish)
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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FS
type: SiteQuality
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ClippingRankSum
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DP
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQ
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QD
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BaseQRankSum
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MQRankSum
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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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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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allele frequency: 0.0e0
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European (Non-Finnish)
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FS
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MQ
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BaseQRankSum
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VQSLOD
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DP
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QD
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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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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Other
type: Population
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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Latino
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BaseQRankSum
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ClippingRankSum
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FS
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MQ
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InbreedingCoeff
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QD
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MQRankSum
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DP
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VQSLOD
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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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bin: 9.25e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2764
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1472
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 5.12935e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.36e-2

QD
type: SiteQuality
SIO_000300: 1.385e1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2216
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 646
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.121830827911151e-4
allele num: 8914
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7686
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.5e-2

QD
type: SiteQuality
SIO_000300: 1.47e0

FS
type: SiteQuality
SIO_000300: 1.018e0

DP
type: SiteQuality
SIO_000300: 5.08454e5

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8914
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2216
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.26e-2

QD
type: SiteQuality
SIO_000300: 1.47e0

FS
type: SiteQuality
SIO_000300: 1.018e0

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.48e-1

DP
type: SiteQuality
SIO_000300: 5.08454e5

VQSLOD
type: SiteQuality
SIO_000300: 5.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2218
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 70
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 1.297690111601349e-4
allele num: 7706
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8940
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.788e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.706e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-2

QD
type: SiteQuality
SIO_000300: 4.72e0

DP
type: SiteQuality
SIO_000300: 5.15496e5

MQRankSum
type: SiteQuality
SIO_000300: -1.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.148e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.51e0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.293995859213251e-4
allele num: 7728
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2222
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 438
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9018
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.23e-2

FS
type: SiteQuality
SIO_000300: 1.758e0

MQRankSum
type: SiteQuality
SIO_000300: -5.1e-1

ReadPosRankSum
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SIO_000300: 5.3e-1

BaseQRankSum
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SIO_000300: -4.71e0

VQSLOD
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SIO_000300: -1.406e0

MQ
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SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.25e1

DP
type: SiteQuality
SIO_000300: 5.29516e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.05e0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9090
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2224
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.479289940828402e-3
allele num: 676
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.018e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.38868e5

VQSLOD
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InbreedingCoeff
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SIO_000300: -6.09e-2

BaseQRankSum
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ClippingRankSum
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SIO_000300: -1.45e-1

ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.923e1

QD
type: SiteQuality
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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

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

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

African
type: Population
allele count: 1
allele frequency: 4.440497335701599e-4
allele num: 2252
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 9248
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 472
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East Asian
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allele count: 0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
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FS
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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DP
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VQSLOD
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 9394
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.41306266548985e-4
allele num: 2266
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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East Asian
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allele count: 0
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allele num: 706
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.022e1

FS
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: -5.45e-2

QD
type: SiteQuality
SIO_000300: 3.16e0

MQRankSum
type: SiteQuality
SIO_000300: -5.209e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.89e0

DP
type: SiteQuality
SIO_000300: 5.65675e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

VQSLOD
type: SiteQuality
SIO_000300: -1.541e0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1777
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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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: 7.5e0
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1287
bin: 6.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7840
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9492
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.28e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.84e0

DP
type: SiteQuality
SIO_000300: 5.73145e5

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 8.73e0

GenotypeQuality
all individuals: 24403
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1268
bin: 6.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 4.044489383215369e-4
allele num: 9890
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2326
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.17e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.21e-2

FS
type: SiteQuality
SIO_000300: 1.0237e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.65e-2

QD
type: SiteQuality
SIO_000300: 1.242e1

DP
type: SiteQuality
SIO_000300: 6.00903e5

GenotypeQuality
all individuals: 1169
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1271
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2443
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 555
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7932
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10114
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.27715996578272e-4
allele num: 2338
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.064e0

QD
type: SiteQuality
SIO_000300: 1.26e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.8e-2

DP
type: SiteQuality
SIO_000300: 6.12088e5

MQ
type: SiteQuality
SIO_000300: 5.878e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.8e-2

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 755
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
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: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7938
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2338
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10184
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.37e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.68e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.869999999999999e0

DP
type: SiteQuality
SIO_000300: 6.13461e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 750
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variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 586
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.255335174491589e-4
allele num: 7966
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2378
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 916
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.253e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.389999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.35e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.3e-1

FS
type: SiteQuality
SIO_000300: 9.419999999999999e-1

DP
type: SiteQuality
SIO_000300: 6.18439e5

VQSLOD
type: SiteQuality
SIO_000300: 8.070000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.09e-1

MQ
type: SiteQuality
SIO_000300: 6.058e1

GenotypeQuality
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bin: 7.5e0
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: 99
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variant carriers: 1

GenotypeQuality
all individuals: 551
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.607717041800643e-3
allele num: 622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7970
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.094091903719912e-3
allele num: 914
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.48e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

MQ
type: SiteQuality
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VQSLOD
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MQRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

ClippingRankSum
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SIO_000300: 1.17e0

FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 8.82e0

BaseQRankSum
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SIO_000300: -1.083e0

DP
type: SiteQuality
SIO_000300: 6.21776e5

GenotypeQuality
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bin: 1.75e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1261
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10416
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.198152812762384e-4
allele num: 2382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7970
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 6.21776e5

QD
type: SiteQuality
SIO_000300: 8.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.083e0

FS
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2726
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7994
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10684
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2410
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 952
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.72e-1

QD
type: SiteQuality
SIO_000300: 1.29e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-2

DP
type: SiteQuality
SIO_000300: 6.2571e5

GenotypeDepth
all individuals: 741
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1529
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 980
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10840
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 4.716981132075472e-3
allele num: 212
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8012
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

FS
type: SiteQuality
SIO_000300: 1.421e0

DP
type: SiteQuality
SIO_000300: 6.2998e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.99e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.87e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.519e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 4.42e0

GenotypeDepth
all individuals: 208
bin: 5.25e1
variant carriers: 0

GenotypeDepth
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bin: 4.25e1
variant carriers: 0

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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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: 6.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 984
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8012
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 9.192866335723479e-5
allele num: 10878
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2428
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.009e1

VQSLOD
type: SiteQuality
SIO_000300: 5.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.15e-1

DP
type: SiteQuality
SIO_000300: 6.31603e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3171
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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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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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 732
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variant carriers: 0

GenotypeQuality
all individuals: 4437
bin: 1.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11956
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1142
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.281e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.64e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.53e-1

DP
type: SiteQuality
SIO_000300: 6.36632e5

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19453
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 140
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GenotypeQuality
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variant carriers: 2

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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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 557
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variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1128
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.322237017310254e-5
allele num: 12016
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8098
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 210
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.903e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.65e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.36122e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -9.366e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17873
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1140
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12294
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.306e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 6.39458e5

QD
type: SiteQuality
SIO_000300: 1.071e1

MQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.422e0

VQSLOD
type: SiteQuality
SIO_000300: -3.242e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.18e-2

FS
type: SiteQuality
SIO_000300: 1.7629e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 728
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2366
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12294
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1140
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 6.39458e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.18e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.7629e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.422e0

QD
type: SiteQuality
SIO_000300: 1.071e1

GenotypeQuality
all individuals: 912
bin: 8.75e1
variant carriers: 836

GenotypeQuality
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bin: 5.25e1
variant carriers: 759

GenotypeQuality
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variant carriers: 1720

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 1546

GenotypeQuality
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bin: 6.75e1
variant carriers: 618

GenotypeQuality
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GenotypeQuality
all individuals: 2534
bin: 1.25e1
variant carriers: 1928

GenotypeQuality
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bin: 3.25e1
variant carriers: 1740

GenotypeQuality
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variant carriers: 603

GenotypeQuality
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variant carriers: 387

GenotypeQuality
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bin: 6.25e1
variant carriers: 853

GenotypeQuality
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variant carriers: 3956

GenotypeQuality
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variant carriers: 986

GenotypeQuality
all individuals: 1119
bin: 9.25e1
variant carriers: 1040

GenotypeQuality
all individuals: 12623
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variant carriers: 12217

GenotypeQuality
all individuals: 590
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variant carriers: 407

GenotypeQuality
all individuals: 536
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variant carriers: 380

GenotypeQuality
all individuals: 7533
bin: 2.25e1
variant carriers: 3495

East Asian
type: Population
allele count: 747
allele frequency: 4.288174512055109e-1
allele num: 1742
num of homozygotes: 108

European (Non-Finnish)
type: Population
allele count: 12595
allele frequency: 6.383679675620882e-1
allele num: 19730
num of homozygotes: 3687

Other
type: Population
allele count: 156
allele frequency: 5.492957746478874e-1
allele num: 284
num of homozygotes: 37

African
type: Population
allele count: 1376
allele frequency: 4.49379490529066e-1
allele num: 3062
num of homozygotes: 274

Latino
type: Population
allele count: 1062
allele frequency: 5.932960893854748e-1
allele num: 1790
num of homozygotes: 244

European (Finnish)
type: Population
allele count: 405
allele frequency: 6.367924528301887e-1
allele num: 636
num of homozygotes: 105

South Asian
type: Population
allele count: 4407
allele frequency: 4.979661016949152e-1
allele num: 8850
num of homozygotes: 1112

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.61e-1

DP
type: SiteQuality
SIO_000300: 7.63156e5

VQSLOD
type: SiteQuality
SIO_000300: 5.91e0

QD
type: SiteQuality
SIO_000300: 2.21e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.561e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

GenotypeQuality
all individuals: 553
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1085
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 109
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5005
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21453
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 3905
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15410
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1339
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2394
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2374
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 317
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8244
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1042
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 240
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

FS
type: SiteQuality
SIO_000300: 3.176e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.683e0

VQSLOD
type: SiteQuality
SIO_000300: -1.374e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.03e-2

DP
type: SiteQuality
SIO_000300: 6.06652e5

QD
type: SiteQuality
SIO_000300: 8.83e0

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15788
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 547
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variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1657
bin: 2.5e0
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GenotypeQuality
all individuals: 3917
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2408
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variant carriers: 0

GenotypeQuality
all individuals: 21837
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GenotypeQuality
all individuals: 187
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 151
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1063
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4165
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2366
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 332
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.588404917286387e-5
allele num: 13178
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1226
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1024
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 238
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8224
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.08e-1

FS
type: SiteQuality
SIO_000300: 6.820000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.64e-2

QD
type: SiteQuality
SIO_000300: 1.66e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

DP
type: SiteQuality
SIO_000300: 6.03301e5

GenotypeQuality
all individuals: 629
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3869
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1416
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22226
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16291
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 880
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3645
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2369
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 113
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2501
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 8.25e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 9.746588693957114e-4
allele num: 1026
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.927729772191673e-4
allele num: 2546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8234
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13174
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1220
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-1

FS
type: SiteQuality
SIO_000300: 1.532e1

VQSLOD
type: SiteQuality
SIO_000300: -1.526e0

DP
type: SiteQuality
SIO_000300: 6.02172e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.66e-2

QD
type: SiteQuality
SIO_000300: 1.438e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeQuality
all individuals: 1416
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16291
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 880
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 113
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3645
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2369
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3869
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22226
bin: 7.5e0
variant carriers: 1

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

GenotypeQuality
all individuals: 629
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2501
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1220
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1026
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

DP
type: SiteQuality
SIO_000300: 6.02172e5

VQSLOD
type: SiteQuality
SIO_000300: -1.526e0

FS
type: SiteQuality
SIO_000300: 1.532e1

QD
type: SiteQuality
SIO_000300: 1.438e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.66e-2

GenotypeQuality
all individuals: 871
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2366
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 630
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variant carriers: 0

GenotypeQuality
all individuals: 16439
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variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.25e1
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GenotypeQuality
all individuals: 1087
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
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GenotypeQuality
all individuals: 22420
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3412
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variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 4.75e1
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GenotypeQuality
all individuals: 333
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variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1204
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 260
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8236
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2536
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 230
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1026
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.00703e5

VQSLOD
type: SiteQuality
SIO_000300: -1.587e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.23e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

QD
type: SiteQuality
SIO_000300: 2.236e1

GenotypeQuality
all individuals: 4249
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1820
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2371
bin: 9.75e1
variant carriers: 8

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 1

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2288
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 171
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1027
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2476
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 8.586849852796859e-4
allele num: 8152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 210
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 932
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1110
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.314e1

FS
type: SiteQuality
SIO_000300: 4.38e-1

DP
type: SiteQuality
SIO_000300: 5.91387e5

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.15e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.36e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 5.25e1
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GenotypeQuality
all individuals: 2342
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1027
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2478
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1120
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8156
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 934
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.616e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.38e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

DP
type: SiteQuality
SIO_000300: 5.91063e5

QD
type: SiteQuality
SIO_000300: 6.55e0

VQSLOD
type: SiteQuality
SIO_000300: -7.091e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 4

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 387
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 335
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 545
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2395
bin: 9.75e1
variant carriers: 35

GenotypeQuality
all individuals: 87
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 298
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 169
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 653
bin: 3.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 36
allele frequency: 2.925877763328999e-3
allele num: 12304
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 4.385964912280702e-3
allele num: 228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 930
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1126
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.454590083456063e-4
allele num: 8148
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 210
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.52e0

DP
type: SiteQuality
SIO_000300: 5.91258e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.85e-2

QD
type: SiteQuality
SIO_000300: 1.237e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.722e0

GenotypeQuality
all individuals: 22842
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4155
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2411
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4066
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1856
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 568
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14654
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2395
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 625
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8148
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 930
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.127438231469441e-5
allele num: 12304
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 210
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.85e-2

QD
type: SiteQuality
SIO_000300: 1.237e1

VQSLOD
type: SiteQuality
SIO_000300: 3.52e0

FS
type: SiteQuality
SIO_000300: 1.722e0

DP
type: SiteQuality
SIO_000300: 5.91258e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

GenotypeDepth
all individuals: 564
bin: 4.75e1
variant carriers: 3

GenotypeDepth
all individuals: 35
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23673
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12823
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4436
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2355
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 188
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2260
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 336
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4652
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2264
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 295
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 974
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 998
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11192
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 8.674101610904585e-4
allele num: 8070
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.356e0

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.75e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.233e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.7652e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.383e0