16-67839430-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67839430
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67839430
    reference: chr 16
allele count: 4
allele frequency: 3.491193464485835e-5
allele num: 114574
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.248A>C
  hgvsp: ENSP00000473396.1:p.Asn83Thr
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.248A>C
  hgvsp: ENSP00000316589.3:p.Asn83Thr
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.248A>C
  hgvsp: ENSP00000473538.1:p.Asn83Thr
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.248A>C
  hgvsp: ENSP00000392808.2:p.Asn83Thr
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-96A>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.248A>C
  hgvsp: ENSP00000473554.1:p.Asn83Thr
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.230A>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-5+775A>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-893A>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.269A>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.235+775A>C
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3555
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15985
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn83Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD

16-67839452-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67839452
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67839452
    reference: chr 16
allele count: 4
allele frequency: 3.964085386399223e-5
allele num: 100906
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.218-10C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-5+753C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.236-10C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.235+753C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.236-10C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-108-10C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.236-10C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-905-10C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.236-10C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.236-10C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.257-10C>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10331
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15645
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

16-67839455-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67839455
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67839455
    reference: chr 16
allele count: 1
allele frequency: 1.009020644562388e-5
allele num: 99106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-5+750C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.236-13C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.236-13C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-108-13C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.236-13C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.236-13C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.257-13C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.218-13C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-905-13C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.236-13C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.235+750C>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9199
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-67839456-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67839456
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67839456
    reference: chr 16
allele count: 9
allele frequency: 9.14281070318373e-5
allele num: 98438
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.236-14C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.218-14C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.236-14C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.235+749C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.236-14C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.257-14C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-108-14C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-5+749C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.236-14C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.236-14C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-905-14C>G
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8893
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12969
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10546
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20196
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ

16-67839479-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67839479
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67839479
    reference: chr 16
allele count: 183
allele frequency: 2.194928874709142e-3
allele num: 83374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-905-37C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.218-37C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-5+726C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.257-37C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.236-37C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.236-37C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.236-37C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-108-37C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.236-37C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.235+726C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.236-37C>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3610
  bin: 2.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6745
  bin: 1.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 3258
  bin: 2.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3509
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14912
  bin: 7.5e0
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 24718
  bin: 1.25e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2745
  bin: 3.75e1
  variant carriers: 2
num of homozygotes: 1
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-67839493-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67839493
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67839493
    reference: chr 16
allele count: 2
allele frequency: 3.027367401307823e-5
allele num: 66064
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.218-51T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.257-51T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.236-51T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.235+712T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-5+712T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.236-51T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.236-51T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.236-51T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.236-51T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-905-51T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-108-51T>C
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4012
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21514
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7051
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3343
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/16-67840161-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840161
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840161
    reference: chr 16
allele count: 1
allele frequency: 2.359269570141084e-5
allele num: 42386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-109+44G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-5+44G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.235+44G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.235+44G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.235+44G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.235+44G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.235+44G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.217+44G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.235+44G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.256+44G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-906+44G>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13003
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10466
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5352
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-67840185-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840185
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840185
    reference: chr 16
allele count: 3
allele frequency: 5.748888548214012e-5
allele num: 52184
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.235+20G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.235+20G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.235+20G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-109+20G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-5+20G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.235+20G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.235+20G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.217+20G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.235+20G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.256+20G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-906+20G>C
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10869
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/16-67840186-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840186
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840186
    reference: chr 16
allele count: 1
allele frequency: 1.888574126534466e-5
allele num: 52950
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-5+19G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.235+19G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-906+19G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.235+19G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-109+19G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.235+19G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.235+19G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.235+19G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.256+19G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.217+19G>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.235+19G>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10610
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30290
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9913
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4015
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/16-67840187-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840187
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840187
    reference: chr 16
allele count: 1
allele frequency: 1.845154623957488e-5
allele num: 54196
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-5+18T>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-906+18T>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-109+18T>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.235+18T>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.235+18T>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.217+18T>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.235+18T>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.235+18T>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.235+18T>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.235+18T>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.256+18T>G
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30091
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10204
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12996
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

16-67840194-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840194
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840194
    reference: chr 16
allele count: 8
allele frequency: 1.306805188016596e-4
allele num: 61218
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.235+11G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.217+11G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.235+11G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-5+11G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.235+11G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.235+11G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.256+11G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-109+11G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-906+11G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.235+11G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.235+11G>A
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27457
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8362
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15712
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

16-67840195-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840195
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840195
    reference: chr 16
allele count: 14
allele frequency: 2.208271554307707e-4
allele num: 63398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.235+10C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.235+10C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-906+10C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-5+10C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.235+10C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.235+10C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-109+10C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.235+10C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.235+10C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.217+10C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.256+10C>G
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17144
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26701
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7856
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2923
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

16-67840198-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840198
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840198
    reference: chr 16
allele count: 1
allele frequency: 1.487077298277965e-5
allele num: 67246
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.235+7G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.217+7G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-5+7G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.235+7G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.256+7G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.235+7G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-109+7G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.235+7G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.235+7G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.235+7G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-906+7G>A
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7099
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25090
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.235+7G>A
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD

16-67840199-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840199
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840199
    reference: chr 16
allele count: 54
allele frequency: 7.831762146482959e-4
allele num: 68950
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-906+6G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.235+6G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.235+6G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.217+6G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-5+6G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.235+6G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.235+6G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.256+6G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.235+6G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-109+6G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.235+6G>C
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6844
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 24309
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20308
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.235+6G>C
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

16-67840202-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840202
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840202
    reference: chr 16
allele count: 1
allele frequency: 1.361804118095653e-5
allele num: 73432
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.217+3A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.256+3A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.235+3A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-109+3A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.235+3A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.235+3A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-906+3A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.235+3A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.235+3A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-5+3A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.235+3A>G
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22616
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.235+3A>G
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

16-67840210-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840210
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840210
    reference: chr 16
allele count: 1
allele frequency: 1.221657544956998e-5
allele num: 81856
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.230A>G
  hgvsp: ENSP00000473396.1:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-911A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-10A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.230A>G
  hgvsp: ENSP00000473395.1:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.230A>G
  hgvsp: ENSP00000392808.2:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.230A>G
  hgvsp: ENSP00000316589.3:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.212A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-114A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.230A>G
  hgvsp: ENSP00000473538.1:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.230A>G
  hgvsp: ENSP00000473554.1:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.251A>G
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18770
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr77Cys
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

16-67840211-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840211
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840211
    reference: chr 16
allele count: 1
allele frequency: 1.209014411451784e-5
allele num: 82712
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.229T>C
  hgvsp: ENSP00000473396.1:p.Tyr77His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.229T>C
  hgvsp: ENSP00000473395.1:p.Tyr77His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-11T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-912T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.229T>C
  hgvsp: ENSP00000392808.2:p.Tyr77His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.229T>C
  hgvsp: ENSP00000473554.1:p.Tyr77His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.229T>C
  hgvsp: ENSP00000473538.1:p.Tyr77His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.229T>C
  hgvsp: ENSP00000316589.3:p.Tyr77His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.211T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-115T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.250T>C
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4552
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28500
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr77His
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

16-67840213-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840213
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840213
    reference: chr 16
allele count: 3
allele frequency: 3.549791745550928e-5
allele num: 84512
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.227A>G
  hgvsp: ENSP00000392808.2:p.His76Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.248A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-117A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.227A>G
  hgvsp: ENSP00000473538.1:p.His76Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.227A>G
  hgvsp: ENSP00000316589.3:p.His76Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.227A>G
  hgvsp: ENSP00000473395.1:p.His76Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-914A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.209A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.227A>G
  hgvsp: ENSP00000473396.1:p.His76Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.227A>G
  hgvsp: ENSP00000473554.1:p.His76Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-13A>G
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5824
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17511
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29411
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His76Arg
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

16-67840214-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840214
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840214
    reference: chr 16
allele count: 1
allele frequency: 1.174094772930071e-5
allele num: 85172
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-118C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.208C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.226C>T
  hgvsp: ENSP00000473395.1:p.His76Tyr
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.226C>T
  hgvsp: ENSP00000316589.3:p.His76Tyr
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.226C>T
  hgvsp: ENSP00000473538.1:p.His76Tyr
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.226C>T
  hgvsp: ENSP00000473396.1:p.His76Tyr
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-915C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.247C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.226C>T
  hgvsp: ENSP00000392808.2:p.His76Tyr
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-14C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.226C>T
  hgvsp: ENSP00000473554.1:p.His76Tyr
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His76Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-67840215-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840215
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840215
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 85954
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-916C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-15C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.225C>T
  hgvsp: ENST00000602815.1:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.207C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.225C>T
  hgvsp: ENST00000602677.1:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.246C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-119C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.225C>T
  hgvsp: ENST00000317506.3:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.225C>T
  hgvsp: ENST00000602638.1:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.225C>T
  hgvsp: ENST00000448631.2:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.225C>T
  hgvsp: ENST00000602506.1:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16848
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val75Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

16-67840218-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840218
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840218
    reference: chr 16
allele count: 4
allele frequency: 4.538955586319588e-5
allele num: 88126
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.222C>T
  hgvsp: ENST00000602506.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-122C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-18C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.222C>T
  hgvsp: ENST00000602677.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.222C>T
  hgvsp: ENST00000602815.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.243C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.222C>T
  hgvsp: ENST00000448631.2:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.222C>T
  hgvsp: ENST00000317506.3:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-919C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.222C>T
  hgvsp: ENST00000602638.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.204C>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15808
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6239
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg74Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

16-67840220-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840220
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840220
    reference: chr 16
allele count: 2
allele frequency: 2.217786648924373e-5
allele num: 90180
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.202C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.241C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.220C>T
  hgvsp: ENSP00000473538.1:p.Arg74Cys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.220C>T
  hgvsp: ENSP00000473554.1:p.Arg74Cys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.220C>T
  hgvsp: ENSP00000473395.1:p.Arg74Cys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.220C>T
  hgvsp: ENSP00000473396.1:p.Arg74Cys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.220C>T
  hgvsp: ENSP00000316589.3:p.Arg74Cys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-124C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.220C>T
  hgvsp: ENSP00000392808.2:p.Arg74Cys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-20C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-921C>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14830
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32434
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg74Cys
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

16-67840221-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840221
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840221
    reference: chr 16
allele count: 37
allele frequency: 4.06888512547562e-4
allele num: 90934
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.219C>T
  hgvsp: ENST00000602638.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.219C>T
  hgvsp: ENST00000602677.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-21C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.219C>T
  hgvsp: ENST00000317506.3:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.219C>T
  hgvsp: ENST00000448631.2:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-125C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.219C>T
  hgvsp: ENST00000602815.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.240C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.219C>T
  hgvsp: ENST00000602506.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-922C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.201C>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6570
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14511
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32745
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu73Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-67840222-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840222
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840222
    reference: chr 16
allele count: 1
allele frequency: 1.09318291136473e-5
allele num: 91476
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.218T>A
  hgvsp: ENSP00000316589.3:p.Leu73His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.200T>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.218T>A
  hgvsp: ENSP00000473554.1:p.Leu73His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.218T>A
  hgvsp: ENSP00000473538.1:p.Leu73His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-126T>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.218T>A
  hgvsp: ENSP00000473395.1:p.Leu73His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.218T>A
  hgvsp: ENSP00000473396.1:p.Leu73His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.239T>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-923T>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.218T>A
  hgvsp: ENSP00000392808.2:p.Leu73His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-22T>A
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33009
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu73His
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

16-67840225-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840225
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840225
    reference: chr 16
allele count: 1
allele frequency: 1.079540547542966e-5
allele num: 92632
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.215A>G
  hgvsp: ENSP00000473554.1:p.Asn72Ser
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.215A>G
  hgvsp: ENSP00000473395.1:p.Asn72Ser
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.215A>G
  hgvsp: ENSP00000473396.1:p.Asn72Ser
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.215A>G
  hgvsp: ENSP00000473538.1:p.Asn72Ser
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.197A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.215A>G
  hgvsp: ENSP00000392808.2:p.Asn72Ser
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.215A>G
  hgvsp: ENSP00000316589.3:p.Asn72Ser
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-25A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.236A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-926A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-129A>G
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13679
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn72Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

16-67840231-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840231
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840231
    reference: chr 16
allele count: 1
allele frequency: 1.044102906782492e-5
allele num: 95776
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.209A>G
  hgvsp: ENSP00000473395.1:p.Gln70Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.209A>G
  hgvsp: ENSP00000473554.1:p.Gln70Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.191A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-932A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-135A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-31A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.209A>G
  hgvsp: ENSP00000392808.2:p.Gln70Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.209A>G
  hgvsp: ENSP00000473396.1:p.Gln70Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.230A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.209A>G
  hgvsp: ENSP00000473538.1:p.Gln70Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.209A>G
  hgvsp: ENSP00000316589.3:p.Gln70Arg
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34660
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln70Arg
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ

16-67840243-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840243
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840243
    reference: chr 16
allele count: 1
allele frequency: 1.01555835398302e-5
allele num: 98468
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-43T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.197T>C
  hgvsp: ENSP00000473554.1:p.Ile66Thr
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.197T>C
  hgvsp: ENSP00000316589.3:p.Ile66Thr
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.197T>C
  hgvsp: ENSP00000473396.1:p.Ile66Thr
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.197T>C
  hgvsp: ENSP00000473395.1:p.Ile66Thr
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.218T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.179T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.197T>C
  hgvsp: ENSP00000473538.1:p.Ile66Thr
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.197T>C
  hgvsp: ENSP00000392808.2:p.Ile66Thr
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-944T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-147T>C
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8144
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10884
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile66Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

16-67840247-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840247
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840247
    reference: chr 16
allele count: 1
allele frequency: 1.00838980316231e-5
allele num: 99168
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.214T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.175T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.193T>C
  hgvsp: ENSP00000392808.2:p.Tyr65His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.193T>C
  hgvsp: ENSP00000316589.3:p.Tyr65His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.193T>C
  hgvsp: ENSP00000473538.1:p.Tyr65His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.193T>C
  hgvsp: ENSP00000473396.1:p.Tyr65His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.193T>C
  hgvsp: ENSP00000473395.1:p.Tyr65His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-47T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.193T>C
  hgvsp: ENSP00000473554.1:p.Tyr65His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-151T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-948T>C
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10537
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr65His
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

16-67840249-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840249
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840249
    reference: chr 16
allele count: 1
allele frequency: 1.008044192657406e-5
allele num: 99202
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-153A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.191A>G
  hgvsp: ENSP00000473538.1:p.Asn64Ser
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.191A>G
  hgvsp: ENSP00000473395.1:p.Asn64Ser
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.191A>G
  hgvsp: ENSP00000316589.3:p.Asn64Ser
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.191A>G
  hgvsp: ENSP00000473396.1:p.Asn64Ser
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.173A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-49A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-950A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.191A>G
  hgvsp: ENSP00000392808.2:p.Asn64Ser
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.191A>G
  hgvsp: ENSP00000473554.1:p.Asn64Ser
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.212A>G
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn64Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD

16-67840259-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840259
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840259
    reference: chr 16
allele count: 1
allele frequency: 1.025872504565133e-5
allele num: 97478
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.181G>A
  hgvsp: ENSP00000392808.2:p.Asp61Asn
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.202G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.181G>A
  hgvsp: ENSP00000473554.1:p.Asp61Asn
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-960G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.181G>A
  hgvsp: ENSP00000473396.1:p.Asp61Asn
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.181G>A
  hgvsp: ENSP00000473538.1:p.Asp61Asn
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.181G>A
  hgvsp: ENSP00000473395.1:p.Asp61Asn
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-59G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.181G>A
  hgvsp: ENSP00000316589.3:p.Asp61Asn
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-163G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.163G>A
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8730
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  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: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4520
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp61Asn
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: C
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

16-67840266-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840266
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840266
    reference: chr 16
allele count: 710
allele frequency: 7.413440253936432e-3
allele num: 95772
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.174C>T
  hgvsp: ENST00000448631.2:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-66C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.174C>T
  hgvsp: ENST00000602815.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.174C>T
  hgvsp: ENST00000602638.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.156C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-170C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.174C>T
  hgvsp: ENST00000317506.3:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.174C>T
  hgvsp: ENST00000602677.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.174C>T
  hgvsp: ENST00000602506.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-967C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.195C>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8667
  bin: 2.75e1
  variant carriers: 147
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29693
  bin: 2.25e1
  variant carriers: 199
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 3.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 1.75e1
  variant carriers: 161
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5814
  bin: 1.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 11939
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 3.25e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Ser58Ser
num of homozygotes: 24
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-67840272-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840272
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840272
    reference: chr 16
allele count: 1
allele frequency: 1.069610234030719e-5
allele num: 93492
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-973C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.189C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.168C>T
  hgvsp: ENST00000448631.2:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.168C>T
  hgvsp: ENST00000602815.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.168C>T
  hgvsp: ENST00000602506.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.168C>T
  hgvsp: ENST00000602677.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.168C>T
  hgvsp: ENST00000602638.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.168C>T
  hgvsp: ENST00000317506.3:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.150C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-72C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-176C>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7060
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13009
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8452
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser56Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP

16-67840283-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840283
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840283
    reference: chr 16
allele count: 1
allele frequency: 1.127726278277736e-5
allele num: 88674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.157C>T
  hgvsp: ENST00000602815.1:c.157C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.178C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.157C>T
  hgvsp: ENST00000602638.1:c.157C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.157C>T
  hgvsp: ENST00000317506.3:c.157C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.157C>T
  hgvsp: ENST00000448631.2:c.157C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-187C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.157C>T
  hgvsp: ENST00000602506.1:c.157C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.139C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.157C>T
  hgvsp: ENST00000602677.1:c.157C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-984C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-83C>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23264
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7669
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu53Leu
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

16-67840290-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840290
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840290
    reference: chr 16
allele count: 107
allele frequency: 1.266811896192461e-3
allele num: 84464
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.171G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.150G>C
  hgvsp: ENSP00000392808.2:p.Glu50Asp
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-194G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.150G>C
  hgvsp: ENSP00000473538.1:p.Glu50Asp
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.150G>C
  hgvsp: ENSP00000473554.1:p.Glu50Asp
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.150G>C
  hgvsp: ENSP00000316589.3:p.Glu50Asp
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-90G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.150G>C
  hgvsp: ENSP00000473395.1:p.Glu50Asp
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.150G>C
  hgvsp: ENSP00000473396.1:p.Glu50Asp
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-991G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.132G>C
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6969
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 1.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 19861
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 11608
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 16824
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
hgvs: p.Glu50Asp
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

16-67840293-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840293
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840293
    reference: chr 16
allele count: 2
allele frequency: 2.421717966725595e-5
allele num: 82586
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.147A>C
  hgvsp: ENSP00000316589.3:p.Gln49His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.168A>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.147A>C
  hgvsp: ENSP00000473538.1:p.Gln49His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.147A>C
  hgvsp: ENSP00000473554.1:p.Gln49His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.147A>C
  hgvsp: ENSP00000473396.1:p.Gln49His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-93A>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.129A>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.147A>C
  hgvsp: ENSP00000473395.1:p.Gln49His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.147A>C
  hgvsp: ENSP00000392808.2:p.Gln49His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-197A>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-994A>C
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18452
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln49His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP

16-67840297-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840297
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840297
    reference: chr 16
allele count: 2
allele frequency: 2.502878310056565e-5
allele num: 79908
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-998A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-201A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.143A>G
  hgvsp: ENSP00000473395.1:p.Gln48Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.143A>G
  hgvsp: ENSP00000473538.1:p.Gln48Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.125A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.143A>G
  hgvsp: ENSP00000473396.1:p.Gln48Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.143A>G
  hgvsp: ENSP00000316589.3:p.Gln48Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.164A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.143A>G
  hgvsp: ENSP00000473554.1:p.Gln48Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.143A>G
  hgvsp: ENSP00000392808.2:p.Gln48Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-97A>G
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13265
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln48Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-67840302-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840302
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840302
    reference: chr 16
allele count: 1
allele frequency: 1.304529325819244e-5
allele num: 76656
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.138C>T
  hgvsp: ENST00000602506.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.138C>T
  hgvsp: ENST00000602638.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-102C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-206C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.138C>T
  hgvsp: ENST00000602815.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.138C>T
  hgvsp: ENST00000602677.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.138C>T
  hgvsp: ENST00000448631.2:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.138C>T
  hgvsp: ENST00000317506.3:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.159C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.120C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1003C>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val46Val
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

16-67840308-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840308
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840308
    reference: chr 16
allele count: 1
allele frequency: 1.395517597476904e-5
allele num: 71658
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.153C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.114C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.132C>T
  hgvsp: ENST00000602638.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.132C>T
  hgvsp: ENST00000317506.3:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.132C>T
  hgvsp: ENST00000602815.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-212C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.132C>T
  hgvsp: ENST00000602506.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.132C>T
  hgvsp: ENST00000602677.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-108C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.132C>T
  hgvsp: ENST00000448631.2:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1009C>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15062
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro44Pro
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum

16-67840328-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840328
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840328
    reference: chr 16
allele count: 5
allele frequency: 9.715906882748436e-5
allele num: 51462
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.94C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.112C>T
  hgvsp: ENSP00000473395.1:p.Arg38Cys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.112C>T
  hgvsp: ENSP00000473554.1:p.Arg38Cys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.112C>T
  hgvsp: ENSP00000473396.1:p.Arg38Cys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1029C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.112C>T
  hgvsp: ENSP00000392808.2:p.Arg38Cys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.112C>T
  hgvsp: ENSP00000316589.3:p.Arg38Cys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-232C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.133C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-128C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.112C>T
  hgvsp: ENSP00000473538.1:p.Arg38Cys
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6051
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24894
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8675
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14494
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg38Cys
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

16-67840329-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840329
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840329
    reference: chr 16
allele count: 2
allele frequency: 3.878675044604763e-5
allele num: 51564
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1030G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.111G>A
  hgvsp: ENST00000602638.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.93G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.111G>A
  hgvsp: ENST00000602506.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.111G>A
  hgvsp: ENST00000448631.2:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-233G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.111G>A
  hgvsp: ENST00000602815.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.111G>A
  hgvsp: ENST00000317506.3:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.132G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-129G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.111G>A
  hgvsp: ENST00000602677.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14393
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg37Arg
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

16-67840331-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840331
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840331
    reference: chr 16
allele count: 7
allele frequency: 1.39955214331414e-4
allele num: 50016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.109C>T
  hgvsp: ENSP00000473538.1:p.Arg37Trp
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.109C>T
  hgvsp: ENSP00000473554.1:p.Arg37Trp
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.91C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.109C>T
  hgvsp: ENSP00000392808.2:p.Arg37Trp
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.109C>T
  hgvsp: ENSP00000473396.1:p.Arg37Trp
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.109C>T
  hgvsp: ENSP00000316589.3:p.Arg37Trp
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.109C>T
  hgvsp: ENSP00000473395.1:p.Arg37Trp
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1032C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.130C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-235C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-131C>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9215
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 25225
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14142
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg37Trp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

16-67840332-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840332
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840332
    reference: chr 16
allele count: 3
allele frequency: 6.071153923989153e-5
allele num: 49414
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.108C>G
  hgvsp: ENSP00000316589.3:p.Ser36Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.108C>G
  hgvsp: ENSP00000473396.1:p.Ser36Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.108C>G
  hgvsp: ENSP00000473395.1:p.Ser36Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.129C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-236C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.108C>G
  hgvsp: ENSP00000473538.1:p.Ser36Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.108C>G
  hgvsp: ENSP00000473554.1:p.Ser36Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1033C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-132C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.108C>G
  hgvsp: ENSP00000392808.2:p.Ser36Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.90C>G
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9538
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13994
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser36Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

16-67840346-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840346
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840346
    reference: chr 16
allele count: 20
allele frequency: 5.070222582771384e-4
allele num: 39446
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.115G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.94G>A
  hgvsp: ENSP00000473396.1:p.Glu32Lys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1047G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.94G>A
  hgvsp: ENSP00000473538.1:p.Glu32Lys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.94G>A
  hgvsp: ENSP00000316589.3:p.Glu32Lys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-250G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.76G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.94G>A
  hgvsp: ENSP00000473395.1:p.Glu32Lys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.94G>A
  hgvsp: ENSP00000392808.2:p.Glu32Lys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.94G>A
  hgvsp: ENSP00000473554.1:p.Glu32Lys
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-146G>A
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14590
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24555
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11391
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu32Lys
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

16-67840349-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840349
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840349
    reference: chr 16
allele count: 1
allele frequency: 2.824380048579337e-5
allele num: 35406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.91G>A
  hgvsp: ENSP00000473396.1:p.Gly31Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.91G>A
  hgvsp: ENSP00000473538.1:p.Gly31Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.91G>A
  hgvsp: ENSP00000473395.1:p.Gly31Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-253G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1050G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.73G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.91G>A
  hgvsp: ENSP00000392808.2:p.Gly31Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.91G>A
  hgvsp: ENSP00000316589.3:p.Gly31Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-149G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.91G>A
  hgvsp: ENSP00000473554.1:p.Gly31Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.112G>A
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly31Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/16-67840350-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840350
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840350
    reference: chr 16
allele count: 1
allele frequency: 2.830615942028986e-5
allele num: 35328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.111T>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1051T>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.72T>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-254T>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.90T>G
  hgvsp: ENST00000602677.1:c.90T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.90T>G
  hgvsp: ENST00000602506.1:c.90T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.90T>G
  hgvsp: ENST00000602638.1:c.90T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.90T>G
  hgvsp: ENST00000317506.3:c.90T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.90T>G
  hgvsp: ENST00000602815.1:c.90T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.90T>G
  hgvsp: ENST00000448631.2:c.90T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-150T>G
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16745
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23752
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10144
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  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: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro30Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

16-67840357-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840357
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840357
    reference: chr 16
allele count: 3
allele frequency: 9.384971532253019e-5
allele num: 31966
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.83C>G
  hgvsp: ENSP00000392808.2:p.Pro28Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.83C>G
  hgvsp: ENSP00000473395.1:p.Pro28Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.83C>G
  hgvsp: ENSP00000473554.1:p.Pro28Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-261C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1058C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.83C>G
  hgvsp: ENSP00000473396.1:p.Pro28Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.83C>G
  hgvsp: ENSP00000316589.3:p.Pro28Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.83C>G
  hgvsp: ENSP00000473538.1:p.Pro28Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.104C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.65C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-157C>G
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23234
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18799
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro28Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS

16-67840357-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840357
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840357
    reference: chr 16
allele count: 1
allele frequency: 3.12832384408434e-5
allele num: 31966
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1058C>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.83C>A
  hgvsp: ENSP00000473396.1:p.Pro28Gln
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.65C>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.83C>A
  hgvsp: ENSP00000473554.1:p.Pro28Gln
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.83C>A
  hgvsp: ENSP00000316589.3:p.Pro28Gln
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-261C>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.83C>A
  hgvsp: ENSP00000473395.1:p.Pro28Gln
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.83C>A
  hgvsp: ENSP00000473538.1:p.Pro28Gln
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-157C>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.104C>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.83C>A
  hgvsp: ENSP00000392808.2:p.Pro28Gln
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23234
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18799
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro28Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

16-67840362-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840362
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840362
    reference: chr 16
allele count: 1
allele frequency: 3.471257983893363e-5
allele num: 28808
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.78G>C
  hgvsp: ENST00000602677.1:c.78G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.78G>C
  hgvsp: ENST00000602815.1:c.78G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-266G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1063G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.99G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.78G>C
  hgvsp: ENST00000448631.2:c.78G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.78G>C
  hgvsp: ENST00000317506.3:c.78G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.78G>C
  hgvsp: ENST00000602506.1:c.78G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.60G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.78G>C
  hgvsp: ENST00000602638.1:c.78G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-162G>C
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7756
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22096
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20895
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly26Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP

16-67840374-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840374
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840374
    reference: chr 16
allele count: 1
allele frequency: 4.896680050925473e-5
allele num: 20422
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.48C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.66C>T
  hgvsp: ENST00000448631.2:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.66C>T
  hgvsp: ENST00000602677.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.66C>T
  hgvsp: ENST00000602638.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.66C>T
  hgvsp: ENST00000317506.3:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.66C>T
  hgvsp: ENST00000602815.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.87C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-278C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1075C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-174C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.66C>T
  hgvsp: ENST00000602506.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19857
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly22Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-67840379-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840379
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840379
    reference: chr 16
allele count: 7
allele frequency: 3.613089707855889e-4
allele num: 19374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.61G>C
  hgvsp: ENSP00000473538.1:p.Gly21Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.61G>C
  hgvsp: ENSP00000473395.1:p.Gly21Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1080G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.61G>C
  hgvsp: ENSP00000473396.1:p.Gly21Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.82G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.61G>C
  hgvsp: ENSP00000316589.3:p.Gly21Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.61G>C
  hgvsp: ENSP00000392808.2:p.Gly21Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.61G>C
  hgvsp: ENSP00000473554.1:p.Gly21Arg
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-283G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-179G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.43G>C
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27553
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19006
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly21Arg
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-67840384-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840384
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840384
    reference: chr 16
allele count: 7
allele frequency: 3.862282056941073e-4
allele num: 18124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.56C>T
  hgvsp: ENSP00000473395.1:p.Ser19Phe
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.56C>T
  hgvsp: ENSP00000392808.2:p.Ser19Phe
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1085C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.38C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.77C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.56C>T
  hgvsp: ENSP00000473396.1:p.Ser19Phe
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.56C>T
  hgvsp: ENSP00000473554.1:p.Ser19Phe
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.56C>T
  hgvsp: ENSP00000316589.3:p.Ser19Phe
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-288C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-184C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.56C>T
  hgvsp: ENSP00000473538.1:p.Ser19Phe
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29014
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18108
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser19Phe
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

16-67840389-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840389
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840389
    reference: chr 16
allele count: 1
allele frequency: 6.00672753483902e-5
allele num: 16648
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.51C>G
  hgvsp: ENSP00000473554.1:p.Asp17Glu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.51C>G
  hgvsp: ENSP00000473396.1:p.Asp17Glu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.72C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-293C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1090C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.51C>G
  hgvsp: ENSP00000473538.1:p.Asp17Glu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.51C>G
  hgvsp: ENSP00000316589.3:p.Asp17Glu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.51C>G
  hgvsp: ENSP00000473395.1:p.Asp17Glu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.51C>G
  hgvsp: ENSP00000392808.2:p.Asp17Glu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-189C>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.33C>G
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16498
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30803
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp17Glu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

16-67840391-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840391
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840391
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 15648
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.49G>A
  hgvsp: ENSP00000316589.3:p.Asp17Asn
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1092G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.49G>A
  hgvsp: ENSP00000473395.1:p.Asp17Asn
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.49G>A
  hgvsp: ENSP00000473554.1:p.Asp17Asn
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.49G>A
  hgvsp: ENSP00000392808.2:p.Asp17Asn
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.31G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.49G>A
  hgvsp: ENSP00000473538.1:p.Asp17Asn
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.70G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.49G>A
  hgvsp: ENSP00000473396.1:p.Asp17Asn
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-191G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-295G>A
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15519
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31642
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp17Asn
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

16-67840396-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840396
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840396
    reference: chr 16
allele count: 1
allele frequency: 6.83433570256971e-5
allele num: 14632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.44C>T
  hgvsp: ENSP00000473396.1:p.Pro15Leu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.44C>T
  hgvsp: ENSP00000473554.1:p.Pro15Leu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.44C>T
  hgvsp: ENSP00000473538.1:p.Pro15Leu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.44C>T
  hgvsp: ENSP00000316589.3:p.Pro15Leu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.26C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.44C>T
  hgvsp: ENSP00000473395.1:p.Pro15Leu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.65C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1097C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-300C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.44C>T
  hgvsp: ENSP00000392808.2:p.Pro15Leu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-196C>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32802
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3463
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro15Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

16-67840396-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840396
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840396
    reference: chr 16
allele count: 1
allele frequency: 6.83433570256971e-5
allele num: 14632
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.44C>A
  hgvsp: ENSP00000316589.3:p.Pro15His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1097C>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.44C>A
  hgvsp: ENSP00000473396.1:p.Pro15His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-196C>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-300C>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.26C>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.65C>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.44C>A
  hgvsp: ENSP00000473554.1:p.Pro15His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.44C>A
  hgvsp: ENSP00000392808.2:p.Pro15His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.44C>A
  hgvsp: ENSP00000473395.1:p.Pro15His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.44C>A
  hgvsp: ENSP00000473538.1:p.Pro15His
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32802
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro15His
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

16-67840417-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840417
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840417
    reference: chr 16
allele count: 1
allele frequency: 1.054185114906177e-4
allele num: 9486
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.23C>T
  hgvsp: ENSP00000473538.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.44C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.23C>T
  hgvsp: ENSP00000473396.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.23C>T
  hgvsp: ENSP00000392808.2:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.23C>T
  hgvsp: ENSP00000473395.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-217C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.23C>T
  hgvsp: ENSP00000473554.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.23C>T
  hgvsp: ENSP00000316589.3:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-321C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1118C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.5C>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9481
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro8Leu
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

16-67840419-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840419
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840419
    reference: chr 16
allele count: 1
allele frequency: 1.140771161305042e-4
allele num: 8766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.21C>T
  hgvsp: ENST00000602677.1:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.21C>T
  hgvsp: ENST00000602815.1:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.21C>T
  hgvsp: ENST00000602638.1:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-219C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.21C>T
  hgvsp: ENST00000448631.2:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.21C>T
  hgvsp: ENST00000317506.3:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.42C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.21C>T
  hgvsp: ENST00000602506.1:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.3C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-323C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1120C>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8826
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp7Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

16-67840421-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840421
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840421
    reference: chr 16
allele count: 2
allele frequency: 2.800336040324839e-4
allele num: 7142
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.19G>C
  hgvsp: ENSP00000473396.1:p.Asp7His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-221G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.19G>C
  hgvsp: ENSP00000473538.1:p.Asp7His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.19G>C
  hgvsp: ENSP00000473395.1:p.Asp7His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.19G>C
  hgvsp: ENSP00000392808.2:p.Asp7His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1122G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.19G>C
  hgvsp: ENSP00000473554.1:p.Asp7His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602887
  gene symbol: RANBP10
  hgvsc: ENST00000602887.1:n.1G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.19G>C
  hgvsp: ENSP00000316589.3:p.Asp7His
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-325G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.40G>C
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7768
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34955
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp7His
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

16-67840422-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840422
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840422
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 7134
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-326A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.18A>G
  hgvsp: ENST00000448631.2:c.18A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.18A>G
  hgvsp: ENST00000602638.1:c.18A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1123A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.18A>G
  hgvsp: ENST00000602506.1:c.18A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.18A>G
  hgvsp: ENST00000602815.1:c.18A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.18A>G
  hgvsp: ENST00000317506.3:c.18A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.18A>G
  hgvsp: ENST00000602677.1:c.18A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-222A>G
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.39A>G
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: synonymous
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7750
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35034
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala6Ala
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

16-67840422-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840422
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840422
    reference: chr 16
allele count: 1
allele frequency: 1.401738155312588e-4
allele num: 7134
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.18A>C
  hgvsp: ENST00000602638.1:c.18A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.18A>C
  hgvsp: ENST00000317506.3:c.18A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1123A>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.39A>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.18A>C
  hgvsp: ENST00000448631.2:c.18A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.18A>C
  hgvsp: ENST00000602506.1:c.18A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-222A>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.18A>C
  hgvsp: ENST00000602677.1:c.18A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-326A>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.18A>C
  hgvsp: ENST00000602815.1:c.18A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35034
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7750
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala6Ala
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

16-67840425-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840425
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840425
    reference: chr 16
allele count: 1
allele frequency: 1.437194596148318e-4
allele num: 6958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-329G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.15G>A
  hgvsp: ENST00000602638.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.15G>A
  hgvsp: ENST00000602815.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1126G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-225G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.36G>A
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.15G>A
  hgvsp: ENST00000448631.2:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.15G>A
  hgvsp: ENST00000602677.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.15G>A
  hgvsp: ENST00000602506.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.15G>A
  hgvsp: ENST00000317506.3:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7764
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7197
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr5Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

16-67840425-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840425
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840425
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 6958
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.15G>C
  hgvsp: ENST00000317506.3:c.15G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.15G>C
  hgvsp: ENST00000602815.1:c.15G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.15G>C
  hgvsp: ENST00000448631.2:c.15G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1126G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.36G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-329G>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.15G>C
  hgvsp: ENST00000602638.1:c.15G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.15G>C
  hgvsp: ENST00000602677.1:c.15G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.15G>C
  hgvsp: ENST00000602506.1:c.15G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-225G>C
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: synonymous
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7764
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr5Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum

16-67840426-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840426
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840426
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 6858
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.14C>T
  hgvsp: ENSP00000473538.1:p.Thr5Met
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.14C>T
  hgvsp: ENSP00000473396.1:p.Thr5Met
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.14C>T
  hgvsp: ENSP00000473554.1:p.Thr5Met
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.14C>T
  hgvsp: ENSP00000316589.3:p.Thr5Met
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-330C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.14C>T
  hgvsp: ENSP00000392808.2:p.Thr5Met
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-226C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.35C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1127C>T
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.14C>T
  hgvsp: ENSP00000473395.1:p.Thr5Met
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35371
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr5Met
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

16-67840456-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840456
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840456
    reference: chr 16
allele count: 1
allele frequency: 3.623188405797101e-4
allele num: 2760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473396
  ensembl transcript: ENST00000602677
  gene symbol: RANBP10
  hgvsc: ENST00000602677.1:c.-17T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473395
  ensembl transcript: ENST00000602815
  gene symbol: RANBP10
  hgvsc: ENST00000602815.1:c.-17T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000392808
  ensembl transcript: ENST00000448631
  gene symbol: RANBP10
  hgvsc: ENST00000448631.2:c.-17T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473554
  ensembl transcript: ENST00000602638
  gene symbol: RANBP10
  hgvsc: ENST00000602638.1:c.-17T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000141084
  ensembl transcript: ENST00000602525
  gene symbol: RANBP10
  hgvsc: ENST00000602525.1:n.5T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000442249
  ensembl transcript: ENST00000536251
  gene symbol: RANBP10
  hgvsc: ENST00000536251.1:c.-1157T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000473538
  ensembl transcript: ENST00000602506
  gene symbol: RANBP10
  hgvsc: ENST00000602506.1:c.-17T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000410617
  ensembl transcript: ENST00000425512
  gene symbol: RANBP10
  hgvsc: ENST00000425512.2:c.-360T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000416460
  ensembl transcript: ENST00000411657
  gene symbol: RANBP10
  hgvsc: ENST00000411657.2:c.-256T>C
  variant of: http://identifiers.org/hgnc/29285
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.-17T>C
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2950
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

16-67840475-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67840475
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67840475
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 1272
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000141084
  ensembl protein: ENSP00000316589
  ensembl transcript: ENST00000317506
  gene symbol: RANBP10
  hgvsc: ENST00000317506.3:c.-36C>T
  variant of: http://identifiers.org/hgnc/29285
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25226
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  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: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1018
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7223
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18353
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 32
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 80
  num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

16-67841016-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67841016
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67841016
    reference: chr 16
allele count: 3
allele frequency: 2.471984179301253e-4
allele num: 12136
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000455640
  ensembl transcript: ENST00000568990
  gene symbol: TSNAXIP1
  hgvsc: ENST00000568990.1:c.-37A>G
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102904
  ensembl transcript: ENST00000487120
  gene symbol: TSNAXIP1
  hgvsc: ENST00000487120.1:n.40A>G
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000457241
  ensembl transcript: ENST00000561639
  gene symbol: TSNAXIP1
  hgvsc: ENST00000561639.1:c.-37A>G
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000463792
  ensembl transcript: ENST00000567852
  gene symbol: TSNAXIP1
  hgvsc: ENST00000567852.1:c.-589A>G
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000454989
  ensembl transcript: ENST00000565148
  gene symbol: TSNAXIP1
  hgvsc: ENST00000565148.1:c.-37A>G
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000411472
  ensembl transcript: ENST00000415766
  gene symbol: TSNAXIP1
  hgvsc: ENST00000415766.3:c.-37A>G
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000458938
  ensembl transcript: ENST00000466164
  gene symbol: TSNAXIP1
  hgvsc: ENST00000466164.1:c.-37A>G
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102904
  ensembl transcript: ENST00000565339
  gene symbol: TSNAXIP1
  hgvsc: ENST00000565339.1:n.23A>G
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000455011
  ensembl transcript: ENST00000563363
  gene symbol: TSNAXIP1
  hgvsc: ENST00000563363.1:c.-37A>G
  variant of: http://identifiers.org/hgnc/18586
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1280
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

16-67841022-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67841022
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67841022
    reference: chr 16
allele count: 1
allele frequency: 8.21962847279303e-5
allele num: 12166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102904
  ensembl transcript: ENST00000487120
  gene symbol: TSNAXIP1
  hgvsc: ENST00000487120.1:n.46C>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000454989
  ensembl transcript: ENST00000565148
  gene symbol: TSNAXIP1
  hgvsc: ENST00000565148.1:c.-31C>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000455640
  ensembl transcript: ENST00000568990
  gene symbol: TSNAXIP1
  hgvsc: ENST00000568990.1:c.-31C>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000411472
  ensembl transcript: ENST00000415766
  gene symbol: TSNAXIP1
  hgvsc: ENST00000415766.3:c.-31C>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000463792
  ensembl transcript: ENST00000567852
  gene symbol: TSNAXIP1
  hgvsc: ENST00000567852.1:c.-583C>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000455011
  ensembl transcript: ENST00000563363
  gene symbol: TSNAXIP1
  hgvsc: ENST00000563363.1:c.-31C>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000458938
  ensembl transcript: ENST00000466164
  gene symbol: TSNAXIP1
  hgvsc: ENST00000466164.1:c.-31C>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000457241
  ensembl transcript: ENST00000561639
  gene symbol: TSNAXIP1
  hgvsc: ENST00000561639.1:c.-31C>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102904
  ensembl transcript: ENST00000565339
  gene symbol: TSNAXIP1
  hgvsc: ENST00000565339.1:n.29C>T
  variant of: http://identifiers.org/hgnc/18586
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1543
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

16-67841042-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67841042
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67841042
    reference: chr 16
allele count: 1
allele frequency: 8.141996417521577e-5
allele num: 12282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102904
  ensembl transcript: ENST00000487120
  gene symbol: TSNAXIP1
  hgvsc: ENST00000487120.1:n.66G>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000464694
  ensembl transcript: ENST00000561654
  gene symbol: TSNAXIP1
  hgvsc: ENST00000561654.1:c.-436G>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000457241
  ensembl transcript: ENST00000561639
  gene symbol: TSNAXIP1
  hgvsc: ENST00000561639.1:c.-11G>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102904
  ensembl transcript: ENST00000565339
  gene symbol: TSNAXIP1
  hgvsc: ENST00000565339.1:n.49G>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000373485
  ensembl transcript: ENST00000388833
  gene symbol: TSNAXIP1
  hgvsc: ENST00000388833.3:c.-362G>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000458938
  ensembl transcript: ENST00000466164
  gene symbol: TSNAXIP1
  hgvsc: ENST00000466164.1:c.-11G>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102904
  ensembl transcript: ENST00000562633
  gene symbol: TSNAXIP1
  hgvsc: ENST00000562633.1:n.13G>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000455011
  ensembl transcript: ENST00000563363
  gene symbol: TSNAXIP1
  hgvsc: ENST00000563363.1:c.-11G>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000455640
  ensembl transcript: ENST00000568990
  gene symbol: TSNAXIP1
  hgvsc: ENST00000568990.1:c.-11G>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000463792
  ensembl transcript: ENST00000567852
  gene symbol: TSNAXIP1
  hgvsc: ENST00000567852.1:c.-563G>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000411472
  ensembl transcript: ENST00000415766
  gene symbol: TSNAXIP1
  hgvsc: ENST00000415766.3:c.-11G>T
  variant of: http://identifiers.org/hgnc/18586
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102904
  ensembl protein: ENSP00000454989
  ensembl transcript: ENST00000565148
  gene symbol: TSNAXIP1
  hgvsc: ENST00000565148.1:c.-11G>T
  variant of: http://identifiers.org/hgnc/18586
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G

GenotypeDepth
all individuals: 134
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6024
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43810
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1664
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 611
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3950
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.565089136847505e-4
allele num: 15594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63330
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8416
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5696
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9928
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10760
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.09e-1

DP
type: SiteQuality
SIO_000300: 1.421433e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.609e0

QD
type: SiteQuality
SIO_000300: 1.512e1

GenotypeQuality
all individuals: 253
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1028
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2799
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 467
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2401
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22511
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24007
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1661
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 398
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2391
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.21240533717995e-5
allele num: 55460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8848
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9046
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4974
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

DP
type: SiteQuality
SIO_000300: 1.142383e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.241e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.769e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.55e-1

QD
type: SiteQuality
SIO_000300: 1.513e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e-1

GenotypeQuality
all individuals: 243
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20789
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24646
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2023
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3209
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1160
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
all individuals: 1656
bin: 9.75e1
variant carriers: 1

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
all individuals: 399
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8928
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.369487811558477e-4
allele num: 7302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14224
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.203e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.203e0

DP
type: SiteQuality
SIO_000300: 1.097584e6

FS
type: SiteQuality
SIO_000300: 3.274e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

MQ
type: SiteQuality
SIO_000300: 5.861e1

VQSLOD
type: SiteQuality
SIO_000300: -1.904e0

QD
type: SiteQuality
SIO_000300: 1.062e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.588e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.22e-1

GenotypeQuality
all individuals: 203
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1964
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
all individuals: 25198
bin: 2.25e1
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GenotypeQuality
all individuals: 310
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.240352811466373e-3
allele num: 7256
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14166
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54032
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4820
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8860
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.88e-1

QD
type: SiteQuality
SIO_000300: 1.451e1

MQRankSum
type: SiteQuality
SIO_000300: -4.62e-1

DP
type: SiteQuality
SIO_000300: 1.084977e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 166
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 378
bin: 8.25e1
variant carriers: 6

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 12

GenotypeQuality
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variant carriers: 182

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 340
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GenotypeQuality
all individuals: 305
bin: 9.25e1
variant carriers: 2

South Asian
type: Population
allele count: 8
allele frequency: 6.202512017367033e-4
allele num: 12898
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 1.374885426214482e-3
allele num: 6546
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.486325211337643e-4
allele num: 4022
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6004
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 6.349206349206349e-3
allele num: 630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 155
allele frequency: 3.416655645196844e-3
allele num: 45366
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 7.587253414264037e-4
allele num: 7908
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-2

DP
type: SiteQuality
SIO_000300: 8.57056e5

FS
type: SiteQuality
SIO_000300: 1.049e0

QD
type: SiteQuality
SIO_000300: 1.406e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

GenotypeQuality
all individuals: 898
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variant carriers: 0

GenotypeQuality
all individuals: 4791
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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: 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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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
all individuals: 261
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variant carriers: 0

GenotypeQuality
all individuals: 5726
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35248
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4420
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3082
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.983293556085919e-4
allele num: 6704
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.64e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 1.454e0

DP
type: SiteQuality
SIO_000300: 7.95585e5

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

QD
type: SiteQuality
SIO_000300: 1.285e1

GenotypeQuality
all individuals: 5149
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
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variant carriers: 0

GenotypeQuality
all individuals: 19498
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 34
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 6365
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variant carriers: 0

GenotypeQuality
all individuals: 137
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GenotypeQuality
all individuals: 53
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GenotypeQuality
all individuals: 4169
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GenotypeQuality
all individuals: 2870
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 1016
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2306
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4076
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.083299305839118e-5
allele num: 24490
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7588
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2364
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1248
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.029e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.78e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

DP
type: SiteQuality
SIO_000300: 5.81919e5

VQSLOD
type: SiteQuality
SIO_000300: -1.637e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.034e0

GenotypeQuality
all individuals: 1982
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 585
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GenotypeQuality
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GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 13
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 6.242197253433209e-4
allele num: 4806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3182
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1728
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29930
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3144
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8994
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.67e0

MQRankSum
type: SiteQuality
SIO_000300: -6.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

DP
type: SiteQuality
SIO_000300: 7.24462e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.800000000000001e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.21e1

GenotypeQuality
all individuals: 1119
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 13
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3256
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9088
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.296848213108268e-5
allele num: 30332
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1750
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.24e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

QD
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.500000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.318e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 7.34518e5

GenotypeQuality
all individuals: 13
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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
all individuals: 918
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GenotypeQuality
all individuals: 33
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GenotypeQuality
all individuals: 1169
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GenotypeQuality
all individuals: 164
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GenotypeQuality
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GenotypeQuality
all individuals: 3994
bin: 3.25e1
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GenotypeQuality
all individuals: 618
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3378
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31042
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.081081081081081e-4
allele num: 9250
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.36e-1

MQRankSum
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SIO_000300: 8.51e-1

DP
type: SiteQuality
SIO_000300: 7.47078e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.5e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3930
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2146
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 1.136363636363636e-4
allele num: 35200
num of homozygotes: 0

African
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allele count: 4
allele frequency: 7.410151908114116e-4
allele num: 5398
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10042
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4040
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 462
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.17e-1

BaseQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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QD
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InbreedingCoeff
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SIO_000300: 7.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4312
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5558
num of homozygotes: 0

European (Non-Finnish)
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allele count: 14
allele frequency: 3.845731238325459e-4
allele num: 36404
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4098
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2244
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.259e1

BaseQRankSum
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ClippingRankSum
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SIO_000300: -4.66e-1

VQSLOD
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FS
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SIO_000300: 1.039e0

MQRankSum
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 6.15e-1

InbreedingCoeff
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SIO_000300: -5.8e-3

DP
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SIO_000300: 8.47671e5

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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bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2410
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4474
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 2.085070892410342e-4
allele num: 4796
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 38646
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

InbreedingCoeff
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SIO_000300: -5.0e-3

FS
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SIO_000300: 1.071e1

VQSLOD
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MQRankSum
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SIO_000300: 9.69e-1

ClippingRankSum
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SIO_000300: 3.23e-1

DP
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SIO_000300: 8.85187e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -1.714e0

QD
type: SiteQuality
SIO_000300: 1.007e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 53

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 54
allele frequency: 1.366396761133603e-3
allele num: 39520
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 5044
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10802
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2506
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.11e-1

ReadPosRankSum
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SIO_000300: 2.71e-1

InbreedingCoeff
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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DP
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QD
type: SiteQuality
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VQSLOD
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SIO_000300: 3.34e0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11328
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6224
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 2.37925291458482e-5
allele num: 42030
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.881e1

MQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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FS
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DP
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BaseQRankSum
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VQSLOD
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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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bin: 3.25e1
variant carriers: 1

African
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allele frequency: 0.0e0
allele num: 6798
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 5772
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.485001485001485e-4
allele num: 6734
num of homozygotes: 0

European (Finnish)
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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

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

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.128293534244243e-5
allele num: 46986
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 6.259911526583758e-5
allele num: 47924
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
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SIO_000300: 1.91e0

MQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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MQ
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DP
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QD
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SIO_000300: 1.165e1

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

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 1.650709805216243e-4
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African
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Other
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MQRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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DP
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MQ
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FS
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

African
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allele frequency: 5.499037668408029e-4
allele num: 7274
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 49758
num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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European (Finnish)
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Other
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DP
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SIO_000300: 1.078689e6

FS
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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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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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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Other
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allele frequency: 0.0e0
allele num: 660
num of homozygotes: 0

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

European (Non-Finnish)
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European (Finnish)
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Latino
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African
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Other
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South Asian
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MQ
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DP
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VQSLOD
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QD
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FS
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3638
num of homozygotes: 0

African
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Latino
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Other
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European (Non-Finnish)
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South Asian
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East Asian
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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QD
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 1.308557969118032e-4
allele num: 7642
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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QD
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ClippingRankSum
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VQSLOD
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MQRankSum
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DP
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InbreedingCoeff
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FS
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ReadPosRankSum
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SIO_000300: 9.5e-1

BaseQRankSum
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SIO_000300: 1.92e0

MQ
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SIO_000300: 5.886e1

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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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 frequency: 0.0e0
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African
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allele frequency: 1.264542235710673e-4
allele num: 7908
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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FS
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.812447892123101e-5
allele num: 55174
num of homozygotes: 0

East Asian
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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BaseQRankSum
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SIO_000300: 2.94e0

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

Latino
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allele frequency: 0.0e0
allele num: 9200
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.800633823105733e-5
allele num: 55536
num of homozygotes: 0

Other
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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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ReadPosRankSum
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SIO_000300: 9.84e-1

MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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FS
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QD
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MQ
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InbreedingCoeff
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7270
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 55532
num of homozygotes: 0

African
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South Asian
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allele frequency: 7.041261794113505e-5
allele num: 14202
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Latino
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allele frequency: 0.0e0
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Other
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ReadPosRankSum
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SIO_000300: -3.67e-1

InbreedingCoeff
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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DP
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VQSLOD
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MQ
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FS
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QD
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9020
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.832105822432304e-5
allele num: 54582
num of homozygotes: 0

African
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European (Finnish)
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South Asian
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East Asian
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DP
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MQ
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BaseQRankSum
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FS
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ReadPosRankSum
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QD
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VQSLOD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 684
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European (Non-Finnish)
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allele frequency: 3.171523450617514e-4
allele num: 53602
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Latino
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allele frequency: 7.296996662958843e-2
allele num: 8990
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European (Finnish)
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East Asian
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South Asian
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African
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QD
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FS
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MQRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
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Other
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.902949571836346e-5
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MQRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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FS
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ClippingRankSum
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QD
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DP
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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

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

African
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allele num: 7324
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Latino
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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VQSLOD
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InbreedingCoeff
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DP
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BaseQRankSum
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FS
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MQ
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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QD
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GenotypeDepth
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variant carriers: 2

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

European (Non-Finnish)
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allele frequency: 4.303481516546887e-5
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num of homozygotes: 0

African
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Latino
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Other
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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MQ
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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FS
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VQSLOD
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DP
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SIO_000300: 9.55383e5

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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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 4.462094507161662e-5
allele num: 44822
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Other
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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East Asian
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African
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VQSLOD
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ClippingRankSum
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MQ
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DP
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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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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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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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Latino
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 42914
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FS
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VQSLOD
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MQ
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QD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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DP
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BaseQRankSum
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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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European (Non-Finnish)
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East Asian
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Latino
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South Asian
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European (Finnish)
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African
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ClippingRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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QD
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DP
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MQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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African
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South Asian
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European (Non-Finnish)
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VQSLOD
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QD
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BaseQRankSum
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FS
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ClippingRankSum
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DP
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InbreedingCoeff
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SIO_000300: -2.07e-2

MQRankSum
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SIO_000300: 2.64e-1

ReadPosRankSum
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SIO_000300: 3.6e-2

MQ
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SIO_000300: 6.0e1

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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Other
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Latino
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East Asian
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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 num: 27734
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European (Finnish)
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South Asian
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BaseQRankSum
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QD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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DP
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VQSLOD
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MQRankSum
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FS
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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European (Non-Finnish)
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allele num: 26890
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South Asian
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African
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East Asian
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Other
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MQRankSum
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SIO_000300: -8.500000000000001e-2

InbreedingCoeff
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MQ
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QD
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FS
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ReadPosRankSum
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DP
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

Latino
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allele frequency: 8.282716731087797e-4
allele num: 3622
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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East Asian
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Other
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ClippingRankSum
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MQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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FS
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BaseQRankSum
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MQ
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QD
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VQSLOD
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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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Latino
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allele frequency: 8.032128514056225e-4
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 8.724311748739822e-4
allele num: 20632
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Other
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East Asian
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European (Finnish)
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South Asian
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MQRankSum
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MQ
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DP
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FS
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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QD
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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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East Asian
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Latino
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African
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European (Non-Finnish)
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Other
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European (Finnish)
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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MQRankSum
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FS
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VQSLOD
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DP
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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African
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Other
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European (Finnish)
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East Asian
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European (Non-Finnish)
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MQ
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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FS
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DP
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VQSLOD
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QD
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InbreedingCoeff
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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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South Asian
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European (Finnish)
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Latino
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African
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East Asian
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European (Non-Finnish)
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Other
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QD
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQ
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MQRankSum
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DP
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BaseQRankSum
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FS
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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: 1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 6.218132073125233e-5
allele num: 16082
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1354
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

MQRankSum
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SIO_000300: 1.43e-1

FS
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QD
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MQ
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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DP
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ClippingRankSum
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SIO_000300: 3.22e-1

BaseQRankSum
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SIO_000300: -5.73e-1

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 9088
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1202
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 7.053180984624065e-5
allele num: 14178
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

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

VQSLOD
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SIO_000300: -3.024e0

InbreedingCoeff
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FS
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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QD
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BaseQRankSum
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SIO_000300: -1.606e0

DP
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SIO_000300: 4.72382e5

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 816
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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.132246376811594e-4
allele num: 8832
num of homozygotes: 0

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

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

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

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

South Asian
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allele frequency: 8.67195242814668e-4
allele num: 8072
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 8234
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.169e1

MQRankSum
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MQ
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BaseQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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DP
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InbreedingCoeff
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SIO_000300: -5.71e-2

ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 166
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

South Asian
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allele frequency: 8.905852417302799e-4
allele num: 7860
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 7502
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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FS
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QD
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ClippingRankSum
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DP
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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allele num: 7550
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Other
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 474
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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South Asian
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East Asian
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Other
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European (Non-Finnish)
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Latino
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VQSLOD
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ClippingRankSum
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FS
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DP
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QD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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South Asian
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East Asian
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African
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European (Finnish)
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Other
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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DP
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FS
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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African
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East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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ClippingRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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DP
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MQ
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QD
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MQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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South Asian
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MQ
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FS
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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VQSLOD
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DP
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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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South Asian
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Other
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Latino
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African
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European (Finnish)
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European (Non-Finnish)
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MQ
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VQSLOD
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FS
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 6.29e-2

QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

DP
type: SiteQuality
SIO_000300: 1.96927e5

GenotypeQuality
all individuals: 273
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2825
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33447
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7197
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2282
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.657e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.29e-2

FS
type: SiteQuality
SIO_000300: 2.593e0

DP
type: SiteQuality
SIO_000300: 1.96927e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 6
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7308
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33626
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2763
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 70
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3366
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 82
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2246
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.588e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.96429e5

FS
type: SiteQuality
SIO_000300: 3.628e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.61e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.04e0

GenotypeQuality
all individuals: 144
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 82
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27574
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3442
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 110
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.754385964912281e-3
allele num: 570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1000
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 960
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.262e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.63e-2

DP
type: SiteQuality
SIO_000300: 1.18868e5

VQSLOD
type: SiteQuality
SIO_000300: -1.535e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 420
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 330
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.1269e4

QD
type: SiteQuality
SIO_000300: 1.409e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.066e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 567
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1507
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 1.630434782608696e-2
allele num: 184
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7504
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.64e-2

FS
type: SiteQuality
SIO_000300: 2.314e0

MQRankSum
type: SiteQuality
SIO_000300: 8.38e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

VQSLOD
type: SiteQuality
SIO_000300: 6.5e-2

DP
type: SiteQuality
SIO_000300: 1.99125e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.443e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.75e-1

QD
type: SiteQuality
SIO_000300: 9.609999999999999e0

GenotypeQuality
all individuals: 690
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 538
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1403
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.329787234042553e-4
allele num: 7520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.403e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.9e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.98e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.00901e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.173e0

QD
type: SiteQuality
SIO_000300: 1.65e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.44e-2

GenotypeDepth
all individuals: 12
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 891
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1450
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 318
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 55
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1655
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.316829075585989e-4
allele num: 7594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0