http://identifiers.org/exac.variant/12-123466606-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466606
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466606
    reference: chr 12
allele count: 3
allele frequency: 2.510166173000653e-5
allele num: 119514
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.548A>C
  hgvsp: ENSP00000396365.2:p.Glu183Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442200
  ensembl transcript: ENST00000542099
  gene symbol: ARL6IP4
  hgvsc: ENST00000542099.1:c.908A>C
  hgvsp: ENSP00000442200.1:p.Glu303Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.107A>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.884A>C
  hgvsp: ENSP00000376230.2:p.Glu295Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.515A>C
  hgvsp: ENSP00000406036.2:p.Glu172Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*64A>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.371A>C
  hgvsp: ENSP00000413132.2:p.Glu124Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.884A>C
  hgvsp: ENSP00000442718.1:p.Glu295Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.518A>C
  hgvsp: ENSP00000391598.2:p.Glu173Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.941A>C
  hgvsp: ENSP00000313422.5:p.Glu314Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.918A>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.934A>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.934A>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.539A>C
  hgvsp: ENSP00000396723.2:p.Glu180Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.548A>C
  hgvsp: ENSP00000441406.1:p.Glu183Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.404A>C
  hgvsp: ENSP00000350532.4:p.Glu135Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.914A>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.404A>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.917A>C
  hgvsp: ENSP00000414847.2:p.Glu306Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5164A>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu314Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-123466607-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466607
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466607
    reference: chr 12
allele count: 1
allele frequency: 8.367920739054759e-6
allele num: 119504
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442200
  ensembl transcript: ENST00000542099
  gene symbol: ARL6IP4
  hgvsc: ENST00000542099.1:c.909G>C
  hgvsp: ENSP00000442200.1:p.Glu303Asp
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.935G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.935G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.918G>C
  hgvsp: ENSP00000414847.2:p.Glu306Asp
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*65G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.885G>C
  hgvsp: ENSP00000376230.2:p.Glu295Asp
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.549G>C
  hgvsp: ENSP00000396365.2:p.Glu183Asp
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.919G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.885G>C
  hgvsp: ENSP00000442718.1:p.Glu295Asp
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.405G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.405G>C
  hgvsp: ENSP00000350532.4:p.Glu135Asp
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.516G>C
  hgvsp: ENSP00000406036.2:p.Glu172Asp
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.942G>C
  hgvsp: ENSP00000313422.5:p.Glu314Asp
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.540G>C
  hgvsp: ENSP00000396723.2:p.Glu180Asp
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.549G>C
  hgvsp: ENSP00000441406.1:p.Glu183Asp
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5165G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.952G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.108G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.372G>C
  hgvsp: ENSP00000413132.2:p.Glu124Asp
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.915G>C
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu314Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

12-123466609-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466609
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466609
    reference: chr 12
allele count: 1
allele frequency: 8.36988181726874e-6
allele num: 119476
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.518C>T
  hgvsp: ENSP00000406036.2:p.Thr173Met
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.374C>T
  hgvsp: ENSP00000413132.2:p.Thr125Met
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.921C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.944C>T
  hgvsp: ENSP00000313422.5:p.Thr315Met
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.937C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.551C>T
  hgvsp: ENSP00000396365.2:p.Thr184Met
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.887C>T
  hgvsp: ENSP00000376230.2:p.Thr296Met
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.954C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.110C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.887C>T
  hgvsp: ENSP00000442718.1:p.Thr296Met
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.542C>T
  hgvsp: ENSP00000396723.2:p.Thr181Met
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.917C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*67C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.920C>T
  hgvsp: ENSP00000414847.2:p.Thr307Met
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5167C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.407C>T
  hgvsp: ENSP00000350532.4:p.Thr136Met
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.937C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.521C>T
  hgvsp: ENSP00000391598.2:p.Thr174Met
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.407C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.551C>T
  hgvsp: ENSP00000441406.1:p.Thr184Met
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr315Met
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

12-123466614-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466614
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466614
    reference: chr 12
allele count: 1
allele frequency: 8.374507997655138e-6
allele num: 119410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.922C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.556C>T
  hgvsp: ENSP00000441406.1:p.Arg186Cys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.523C>T
  hgvsp: ENSP00000406036.2:p.Arg175Cys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5172C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.526C>T
  hgvsp: ENSP00000391598.2:p.Arg176Cys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.926C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.556C>T
  hgvsp: ENSP00000396365.2:p.Arg186Cys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.925C>T
  hgvsp: ENSP00000414847.2:p.Arg309Cys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.412C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442200
  ensembl transcript: ENST00000542099
  gene symbol: ARL6IP4
  hgvsc: ENST00000542099.1:c.916C>T
  hgvsp: ENSP00000442200.1:p.Arg306Cys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.547C>T
  hgvsp: ENSP00000396723.2:p.Arg183Cys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.412C>T
  hgvsp: ENSP00000350532.4:p.Arg138Cys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.379C>T
  hgvsp: ENSP00000413132.2:p.Arg127Cys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.892C>T
  hgvsp: ENSP00000376230.2:p.Arg298Cys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.892C>T
  hgvsp: ENSP00000442718.1:p.Arg298Cys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.942C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.949C>T
  hgvsp: ENSP00000313422.5:p.Arg317Cys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.942C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*72C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.115C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg317Cys
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

12-123466615-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466615
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466615
    reference: chr 12
allele count: 10
allele frequency: 8.377314233056883e-5
allele num: 119370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.527G>A
  hgvsp: ENSP00000391598.2:p.Arg176His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.960G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.557G>A
  hgvsp: ENSP00000441406.1:p.Arg186His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.893G>A
  hgvsp: ENSP00000442718.1:p.Arg298His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.557G>A
  hgvsp: ENSP00000396365.2:p.Arg186His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.524G>A
  hgvsp: ENSP00000406036.2:p.Arg175His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*73G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.380G>A
  hgvsp: ENSP00000413132.2:p.Arg127His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5173G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.413G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.923G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.548G>A
  hgvsp: ENSP00000396723.2:p.Arg183His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.950G>A
  hgvsp: ENSP00000313422.5:p.Arg317His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.413G>A
  hgvsp: ENSP00000350532.4:p.Arg138His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442200
  ensembl transcript: ENST00000542099
  gene symbol: ARL6IP4
  hgvsc: ENST00000542099.1:c.917G>A
  hgvsp: ENSP00000442200.1:p.Arg306His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.943G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.893G>A
  hgvsp: ENSP00000376230.2:p.Arg298His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.943G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.116G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.926G>A
  hgvsp: ENSP00000414847.2:p.Arg309His
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg317His
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

12-123466617-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466617
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466617
    reference: chr 12
allele count: 1
allele frequency: 8.378156470450242e-6
allele num: 119358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.928A>G
  hgvsp: ENSP00000414847.2:p.Thr310Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.945A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.415A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.415A>G
  hgvsp: ENSP00000350532.4:p.Thr139Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.559A>G
  hgvsp: ENSP00000396365.2:p.Thr187Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442200
  ensembl transcript: ENST00000542099
  gene symbol: ARL6IP4
  hgvsc: ENST00000542099.1:c.919A>G
  hgvsp: ENSP00000442200.1:p.Thr307Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*75A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.895A>G
  hgvsp: ENSP00000442718.1:p.Thr299Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5175A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.559A>G
  hgvsp: ENSP00000441406.1:p.Thr187Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.550A>G
  hgvsp: ENSP00000396723.2:p.Thr184Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.526A>G
  hgvsp: ENSP00000406036.2:p.Thr176Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.382A>G
  hgvsp: ENSP00000413132.2:p.Thr128Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.895A>G
  hgvsp: ENSP00000376230.2:p.Thr299Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.962A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.952A>G
  hgvsp: ENSP00000313422.5:p.Thr318Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.929A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.529A>G
  hgvsp: ENSP00000391598.2:p.Thr177Ala
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.925A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.118A>G
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr318Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ

12-123466621-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466621
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466621
    reference: chr 12
allele count: 2
allele frequency: 1.676502145922747e-5
allele num: 119296
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.956G>C
  hgvsp: ENSP00000313422.5:p.Arg319Thr
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.563G>C
  hgvsp: ENSP00000441406.1:p.Arg188Thr
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.563G>C
  hgvsp: ENSP00000396365.2:p.Arg188Thr
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.419G>C
  hgvsp: ENSP00000350532.4:p.Arg140Thr
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.949G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.929G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.933G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.899G>C
  hgvsp: ENSP00000442718.1:p.Arg300Thr
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.899G>C
  hgvsp: ENSP00000376230.2:p.Arg300Thr
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.949G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.419G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.122G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.386G>C
  hgvsp: ENSP00000413132.2:p.Arg129Thr
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*79G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.554G>C
  hgvsp: ENSP00000396723.2:p.Arg185Thr
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.932G>C
  hgvsp: ENSP00000414847.2:p.Arg311Thr
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.530G>C
  hgvsp: ENSP00000406036.2:p.Arg177Thr
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5179G>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg319Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

12-123466627-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466627
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466627
    reference: chr 12
allele count: 1
allele frequency: 8.392500461587526e-6
allele num: 119154
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.956+6G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.955G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.563+6G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.899+6G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.563+6G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.932+6G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5179+6G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.972G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.899+6G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.386+6G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.533+6G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.949+6G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.122+6G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.419+6G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.554+6G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*79+6G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.530+6G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.419+6G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.939G>A
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: n.5179+6G>A
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-123466634-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466634
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466634
    reference: chr 12
allele count: 5
allele frequency: 4.200268817204301e-5
allele num: 119040
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.122+13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.386+13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.956+13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.932+13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.530+13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.929+13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.946C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.533+13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.979C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*79+13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.962C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.899+13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.949+13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.419+13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.563+13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5179+13C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.419+13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.554+13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.899+13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.563+13C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

12-123466635-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466635
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466635
    reference: chr 12
allele count: 2
allele frequency: 1.680531047811108e-5
allele num: 119010
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*79+14G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.386+14G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.419+14G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.899+14G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.563+14G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.956+14G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.980G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.563+14G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.963G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.929+14G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.533+14G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.554+14G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.947G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.122+14G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.932+14G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.949+14G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.530+14G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.419+14G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5179+14G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.899+14G>A
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum

12-123466640-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466640
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466640
    reference: chr 12
allele count: 2
allele frequency: 1.681011296395912e-5
allele num: 118976
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.899+19G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.554+19G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.419+19G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.956+19G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.899+19G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.968G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.932+19G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.386+19G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.563+19G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5179+19G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.563+19G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*79+19G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.985G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.949+19G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.122+19G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.952G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.533+19G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.929+19G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.530+19G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.419+19G>C
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

12-123466644-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466644
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466645
    reference: chr 12
allele count: 1
allele frequency: 8.40745909771149e-6
allele num: 118942
alternate allele: TA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.956+24dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.122+24dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.563+24dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.563+24dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.949+24dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.973dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.899+24dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.533+24dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.957dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.990dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.419+24dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.899+24dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.932+24dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.530+24dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.419+24dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*79+24dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.554+24dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.929+24dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.386+24dupA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5179+24dupA
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

12-123466646-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466646
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466646
    reference: chr 12
allele count: 4
allele frequency: 3.364228161953944e-5
allele num: 118898
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.419+25C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.563+25C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5179+25C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.554+25C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.974C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.419+25C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.530+25C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.122+25C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.563+25C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.899+25C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.991C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.386+25C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*79+25C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.533+25C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.899+25C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.958C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.932+25C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.929+25C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.949+25C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.956+25C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD

12-123466647-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466647
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466647
    reference: chr 12
allele count: 1
allele frequency: 8.411843876177658e-6
allele num: 118880
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.949+26A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.975A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.563+26A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.959A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.992A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.899+26A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.554+26A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*79+26A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5179+26A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.899+26A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.419+26A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.386+26A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.533+26A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.956+26A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.122+26A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.419+26A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.530+26A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.929+26A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.563+26A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.932+26A>G
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

12-123466652-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466652
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466652
    reference: chr 12
allele count: 1
allele frequency: 8.418358756776778e-6
allele num: 118788
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.949+31A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.899+31A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*79+31A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.899+31A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.932+31A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.956+31A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.980A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.964A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.419+31A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.554+31A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.997A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.929+31A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.563+31A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.386+31A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5179+31A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.530+31A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.419+31A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.122+31A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.563+31A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.533+31A>G
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

12-123466662-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466662
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466662
    reference: chr 12
allele count: 18
allele frequency: 1.516964722142628e-4
allele num: 118658
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.563+41A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.533+41A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.386+41A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.419+41A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.530+41A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.949+41A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.974A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.563+41A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.554+41A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1007A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.899+41A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.990A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*79+41A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.419+41A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.929+41A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.899+41A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5179+41A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.122+41A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.932+41A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.956+41A>G
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13875
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

12-123466664-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466664
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466664
    reference: chr 12
allele count: 1
allele frequency: 8.430281571404485e-6
allele num: 118620
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.419+43T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.386+43T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.530+43T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.976T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.122+43T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.899+43T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.554+43T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.932+43T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.956+43T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.992T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.563+43T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*79+43T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.419+43T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5179+43T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.949+43T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.563+43T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.929+43T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.899+43T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1009T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.533+43T>C
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-123466666-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466666
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466666
    reference: chr 12
allele count: 108
allele frequency: 9.108082579948725e-4
allele num: 118576
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*79+45T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.949+45T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.530+45T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.978T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.994T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.956+45T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.122+45T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.554+45T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.386+45T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.932+45T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1011T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.563+45T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.533+45T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.929+45T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.899+45T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.563+45T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.419+45T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5179+45T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.899+45T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.419+45T>C
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 3.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
num of homozygotes: 2
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

12-123466970-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466970
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466970
    reference: chr 12
allele count: 1
allele frequency: 2.006340034509049e-5
allele num: 49842
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.900-46G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1298G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*80-46G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5180-46G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.420-46G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.564-46G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.957-46G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1282G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.387-46G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.123-46G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.534-46G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.555-46G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.564-46G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.900-46G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1315G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.420-46G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.930-46G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.531-46G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.933-46G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.950-46G>A
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

12-123466974-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466974
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466974
    reference: chr 12
allele count: 1
allele frequency: 1.975191593584578e-5
allele num: 50628
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.420-42A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.900-42A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1302A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.950-42A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1319A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.564-42A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.933-42A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.420-42A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*80-42A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.900-42A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.387-42A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.555-42A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.564-42A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1286A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.531-42A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.957-42A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.930-42A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.534-42A>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5180-42A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.123-42A>T
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-123466977-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466977
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466977
    reference: chr 12
allele count: 2
allele frequency: 3.87551835057939e-5
allele num: 51606
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1305T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.387-39T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.900-39T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.957-39T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.933-39T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.930-39T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1289T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.564-39T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1322T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.555-39T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*80-39T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.123-39T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.564-39T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.534-39T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5180-39T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.900-39T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.420-39T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.531-39T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.420-39T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.950-39T>C
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/12-123466979-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466979
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466979
    reference: chr 12
allele count: 1
allele frequency: 1.928268414963363e-5
allele num: 51860
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.420-37C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1291C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5180-37C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.900-37C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.957-37C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.933-37C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.420-37C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.564-37C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.930-37C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1324C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.531-37C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1307C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.387-37C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.564-37C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.123-37C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.900-37C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.555-37C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.950-37C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.534-37C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*80-37C>A
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum

12-123466982-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466982
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466982
    reference: chr 12
allele count: 1
allele frequency: 1.893580761219466e-5
allele num: 52810
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.531-34A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1294A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.930-34A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*80-34A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.123-34A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.420-34A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.564-34A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5180-34A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.387-34A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.900-34A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.555-34A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.950-34A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.933-34A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1327A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1310A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.957-34A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.420-34A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.900-34A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.534-34A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.564-34A>G
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

12-123466985-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466985
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466985
    reference: chr 12
allele count: 2
allele frequency: 3.732178846010301e-5
allele num: 53588
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.957-31C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1330C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.531-31C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.950-31C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.933-31C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.564-31C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.534-31C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*80-31C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.900-31C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.387-31C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1313C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.420-31C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1297C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.555-31C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.900-31C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.420-31C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.564-31C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.930-31C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5180-31C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.123-31C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

12-123466986-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466986
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466986
    reference: chr 12
allele count: 1
allele frequency: 1.848975667480216e-5
allele num: 54084
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.387-30C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.123-30C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.900-30C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.531-30C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.957-30C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1314C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.420-30C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1298C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.564-30C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1331C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.420-30C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.564-30C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*80-30C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.933-30C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.534-30C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5180-30C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.930-30C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.555-30C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.950-30C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.900-30C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/12-123466995-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466995
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466995
    reference: chr 12
allele count: 1
allele frequency: 1.676558360996546e-5
allele num: 59646
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.950-21C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.564-21C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5180-21C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1307C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.930-21C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.123-21C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1340C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*80-21C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.564-21C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.420-21C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1323C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.900-21C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.555-21C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.531-21C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.420-21C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.933-21C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.957-21C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.387-21C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.900-21C>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.534-21C>A
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

12-123466995-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466995
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466995
    reference: chr 12
allele count: 3
allele frequency: 5.029675082989639e-5
allele num: 59646
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.564-21C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.564-21C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1323C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.534-21C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.420-21C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.900-21C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*80-21C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.933-21C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.555-21C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.957-21C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1340C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1307C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.900-21C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.123-21C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.387-21C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5180-21C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.930-21C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.531-21C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.950-21C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.420-21C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

12-123466996-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123466996
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123466996
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 62180
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.900-20G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.420-20G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1341G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.123-20G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1324G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.900-20G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.531-20G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.564-20G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.564-20G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.387-20G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.930-20G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1308G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.555-20G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5180-20G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.957-20G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.420-20G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.950-20G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.534-20G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.933-20G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*80-20G>A
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

12-123467001-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467001
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467001
    reference: chr 12
allele count: 1
allele frequency: 1.461133839859731e-5
allele num: 68440
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5180-15C>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.957-15C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.564-15C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.387-15C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.420-15C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1329C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.933-15C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.900-15C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.123-15C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1313C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1346C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.420-15C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.555-15C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.950-15C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.531-15C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.900-15C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*80-15C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.930-15C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.564-15C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.534-15C>G
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16362
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

12-123467001-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467001
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467001
    reference: chr 12
allele count: 1
allele frequency: 1.461133839859731e-5
allele num: 68440
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.957-15C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.564-15C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.933-15C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.534-15C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5180-15C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*80-15C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1329C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.123-15C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.900-15C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1346C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.420-15C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1313C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.387-15C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.930-15C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.900-15C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.564-15C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.420-15C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.950-15C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.531-15C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.555-15C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

12-123467003-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467003
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467003
    reference: chr 12
allele count: 1
allele frequency: 1.394505647747873e-5
allele num: 71710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.420-13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.420-13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.933-13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.555-13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1331C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.957-13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1315C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.900-13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1348C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.534-13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.564-13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.531-13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.900-13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.387-13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*80-13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.564-13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.930-13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.950-13C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5180-13C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.123-13C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

12-123467005-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467005
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467005
    reference: chr 12
allele count: 2
allele frequency: 2.690196922414721e-5
allele num: 74344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.555-11C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.957-11C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1317C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.933-11C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.420-11C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.123-11C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.564-11C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1350C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.950-11C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.900-11C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.387-11C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.900-11C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.564-11C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*80-11C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.531-11C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5180-11C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.534-11C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1333C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.930-11C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.420-11C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-123467010-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467010
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467010
    reference: chr 12
allele count: 1
allele frequency: 1.230557196298484e-5
allele num: 81264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.387-6C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.420-6C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5180-6C>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.933-6C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.123-6C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.900-6C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.555-6C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1355C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.564-6C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*80-6C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.930-6C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.564-6C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.420-6C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1338C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.534-6C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.900-6C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.957-6C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1322C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.950-6C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: n.5180-6C>T
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP

12-123467013-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467013
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467013
    reference: chr 12
allele count: 3
allele frequency: 3.489021213248976e-5
allele num: 85984
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.564-3C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*80-3C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.950-3C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.387-3C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.900-3C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1341C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.123-3C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.531-3C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.420-3C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.534-3C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1358C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5180-3C>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.900-3C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.957-3C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.555-3C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.420-3C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1325C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.933-3C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.930-3C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: n.5180-3C>T
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

12-123467017-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467017
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467017
    reference: chr 12
allele count: 3
allele frequency: 3.25754120789628e-5
allele num: 92094
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.901C>T
  hgvsp: ENSP00000442718.1:p.Leu301Phe
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.934C>T
  hgvsp: ENSP00000414847.2:p.Leu312Phe
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.421C>T
  hgvsp: ENSP00000350532.4:p.Leu141Phe
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.388C>T
  hgvsp: ENSP00000413132.2:p.Leu130Phe
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.532C>T
  hgvsp: ENSP00000406036.2:p.Leu178Phe
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5181C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.951C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.565C>T
  hgvsp: ENSP00000441406.1:p.Leu189Phe
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.421C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.901C>T
  hgvsp: ENSP00000376230.2:p.Leu301Phe
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.958C>T
  hgvsp: ENSP00000313422.5:p.Leu320Phe
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1345C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.556C>T
  hgvsp: ENSP00000396723.2:p.Leu186Phe
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1362C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.124C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.565C>T
  hgvsp: ENSP00000396365.2:p.Leu189Phe
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.535C>T
  hgvsp: ENSP00000391598.2:p.Leu179Phe
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*81C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu320Phe
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

12-123467019-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467019
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467019
    reference: chr 12
allele count: 9
allele frequency: 9.378712406994436e-5
allele num: 95962
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.933T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.903T>C
  hgvsp: ENST00000543566.1:c.903T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.534T>C
  hgvsp: ENST00000426960.2:c.534T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1364T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.936T>C
  hgvsp: ENST00000453766.2:c.936T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.960T>C
  hgvsp: ENST00000315580.5:c.960T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.537T>C
  hgvsp: ENST00000456762.2:c.537T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.903T>C
  hgvsp: ENST00000392435.2:c.903T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.953T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.558T>C
  hgvsp: ENST00000454885.2:c.558T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.390T>C
  hgvsp: ENST00000412505.2:c.390T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.126T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1347T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.423T>C
  hgvsp: ENST00000357866.4:c.423T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5183T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.423T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*83T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1331T>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.567T>C
  hgvsp: ENST00000439686.2:c.567T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.567T>C
  hgvsp: ENST00000413381.2:c.567T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu320Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

12-123467032-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467032
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467032
    reference: chr 12
allele count: 1
allele frequency: 9.081497357284268e-6
allele num: 110114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1377G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.580G>A
  hgvsp: ENSP00000441406.1:p.Gly194Ser
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.571G>A
  hgvsp: ENSP00000396723.2:p.Gly191Ser
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.436G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.916G>A
  hgvsp: ENSP00000376230.2:p.Gly306Ser
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.973G>A
  hgvsp: ENSP00000313422.5:p.Gly325Ser
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.436G>A
  hgvsp: ENSP00000350532.4:p.Gly146Ser
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*96G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.946G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.949G>A
  hgvsp: ENSP00000414847.2:p.Gly317Ser
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.547G>A
  hgvsp: ENSP00000406036.2:p.Gly183Ser
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.580G>A
  hgvsp: ENSP00000396365.2:p.Gly194Ser
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.403G>A
  hgvsp: ENSP00000413132.2:p.Gly135Ser
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.916G>A
  hgvsp: ENSP00000442718.1:p.Gly306Ser
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1344G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5196G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.139G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.966G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.550G>A
  hgvsp: ENSP00000391598.2:p.Gly184Ser
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1360G>A
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly325Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

12-123467034-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467034
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467034
    reference: chr 12
allele count: 1
allele frequency: 8.968288133161142e-6
allele num: 111504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.948C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.573C>T
  hgvsp: ENST00000454885.2:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.582C>T
  hgvsp: ENST00000439686.2:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1379C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.405C>T
  hgvsp: ENST00000412505.2:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.968C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.582C>T
  hgvsp: ENST00000413381.2:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.975C>T
  hgvsp: ENST00000315580.5:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.951C>T
  hgvsp: ENST00000453766.2:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.549C>T
  hgvsp: ENST00000426960.2:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*98C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5198C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1362C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.438C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.918C>T
  hgvsp: ENST00000543566.1:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.918C>T
  hgvsp: ENST00000392435.2:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.552C>T
  hgvsp: ENST00000456762.2:c.552C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1346C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.438C>T
  hgvsp: ENST00000357866.4:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.141C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly325Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-123467035-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467035
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467035
    reference: chr 12
allele count: 1
allele frequency: 8.818964300832511e-6
allele num: 113392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.583G>A
  hgvsp: ENSP00000441406.1:p.Glu195Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.976G>A
  hgvsp: ENSP00000313422.5:p.Glu326Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.553G>A
  hgvsp: ENSP00000391598.2:p.Glu185Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.550G>A
  hgvsp: ENSP00000406036.2:p.Glu184Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.919G>A
  hgvsp: ENSP00000442718.1:p.Glu307Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.583G>A
  hgvsp: ENSP00000396365.2:p.Glu195Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.919G>A
  hgvsp: ENSP00000376230.2:p.Glu307Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.142G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.952G>A
  hgvsp: ENSP00000414847.2:p.Glu318Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1363G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.406G>A
  hgvsp: ENSP00000413132.2:p.Glu136Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.574G>A
  hgvsp: ENSP00000396723.2:p.Glu192Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5199G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*99G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.439G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.949G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.439G>A
  hgvsp: ENSP00000350532.4:p.Glu147Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.969G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1347G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1380G>A
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu326Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

12-123467040-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467040
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467040
    reference: chr 12
allele count: 28
allele frequency: 2.405704957470573e-4
allele num: 116390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.558C>T
  hgvsp: ENST00000456762.2:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.588C>T
  hgvsp: ENST00000439686.2:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5204C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.588C>T
  hgvsp: ENST00000413381.2:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.579C>T
  hgvsp: ENST00000454885.2:c.579C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.924C>T
  hgvsp: ENST00000543566.1:c.924C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.957C>T
  hgvsp: ENST00000453766.2:c.957C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*104C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.411C>T
  hgvsp: ENST00000412505.2:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.924C>T
  hgvsp: ENST00000392435.2:c.924C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.147C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1368C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.555C>T
  hgvsp: ENST00000426960.2:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.981C>T
  hgvsp: ENST00000315580.5:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.954C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.444C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1385C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.444C>T
  hgvsp: ENST00000357866.4:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.974C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1352C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val327Val
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

12-123467043-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467043
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467043
    reference: chr 12
allele count: 1
allele frequency: 8.508465923593976e-6
allele num: 117530
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.957A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.591A>G
  hgvsp: ENST00000413381.2:c.591A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.558A>G
  hgvsp: ENST00000426960.2:c.558A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.927A>G
  hgvsp: ENST00000392435.2:c.927A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.591A>G
  hgvsp: ENST00000439686.2:c.591A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.561A>G
  hgvsp: ENST00000456762.2:c.561A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.984A>G
  hgvsp: ENST00000315580.5:c.984A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1371A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.582A>G
  hgvsp: ENST00000454885.2:c.582A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.150A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.960A>G
  hgvsp: ENST00000453766.2:c.960A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.447A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1355A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.927A>G
  hgvsp: ENST00000543566.1:c.927A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.447A>G
  hgvsp: ENST00000357866.4:c.447A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.414A>G
  hgvsp: ENST00000412505.2:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1388A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5207A>G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*107A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.977A>G
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu328Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

12-123467047-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467047
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467047
    reference: chr 12
allele count: 1
allele frequency: 8.43340979624882e-6
allele num: 118576
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.586G>A
  hgvsp: ENSP00000396723.2:p.Glu196Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.931G>A
  hgvsp: ENSP00000376230.2:p.Glu311Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5211G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.451G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.988G>A
  hgvsp: ENSP00000313422.5:p.Glu330Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.931G>A
  hgvsp: ENSP00000442718.1:p.Glu311Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.964G>A
  hgvsp: ENSP00000414847.2:p.Glu322Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*111G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.961G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.154G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.562G>A
  hgvsp: ENSP00000406036.2:p.Glu188Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.565G>A
  hgvsp: ENSP00000391598.2:p.Glu189Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.451G>A
  hgvsp: ENSP00000350532.4:p.Glu151Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.418G>A
  hgvsp: ENSP00000413132.2:p.Glu140Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1392G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1375G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.595G>A
  hgvsp: ENSP00000396365.2:p.Glu199Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1359G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.981G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.595G>A
  hgvsp: ENSP00000441406.1:p.Glu199Lys
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu330Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

12-123467052-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467052
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467052
    reference: chr 12
allele count: 5
allele frequency: 4.191325632471038e-5
allele num: 119294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.966C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1380C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.936C>T
  hgvsp: ENST00000543566.1:c.936C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1364C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.159C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.600C>T
  hgvsp: ENST00000439686.2:c.600C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.567C>T
  hgvsp: ENST00000426960.2:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.456C>T
  hgvsp: ENST00000357866.4:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.570C>T
  hgvsp: ENST00000456762.2:c.570C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1397C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.591C>T
  hgvsp: ENST00000454885.2:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5216C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*116C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.969C>T
  hgvsp: ENST00000453766.2:c.969C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.936C>T
  hgvsp: ENST00000392435.2:c.936C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.993C>T
  hgvsp: ENST00000315580.5:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.600C>T
  hgvsp: ENST00000413381.2:c.600C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.456C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.423C>T
  hgvsp: ENST00000412505.2:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.986C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile331Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-123467053-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467053
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467053
    reference: chr 12
allele count: 2
allele frequency: 1.674032409267444e-5
allele num: 119472
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.601G>A
  hgvsp: ENSP00000441406.1:p.Val201Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.592G>A
  hgvsp: ENSP00000396723.2:p.Val198Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.424G>A
  hgvsp: ENSP00000413132.2:p.Val142Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.601G>A
  hgvsp: ENSP00000396365.2:p.Val201Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*117G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1381G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.937G>A
  hgvsp: ENSP00000376230.2:p.Val313Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.937G>A
  hgvsp: ENSP00000442718.1:p.Val313Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1398G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.994G>A
  hgvsp: ENSP00000313422.5:p.Val332Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.568G>A
  hgvsp: ENSP00000406036.2:p.Val190Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.457G>A
  hgvsp: ENSP00000350532.4:p.Val153Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.571G>A
  hgvsp: ENSP00000391598.2:p.Val191Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.457G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.970G>A
  hgvsp: ENSP00000414847.2:p.Val324Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.160G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1365G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.987G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5217G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.967G>A
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val332Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

12-123467057-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467057
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467057
    reference: chr 12
allele count: 1
allele frequency: 8.341675008341675e-6
allele num: 119880
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.605C>T
  hgvsp: ENSP00000396365.2:p.Thr202Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.572C>T
  hgvsp: ENSP00000406036.2:p.Thr191Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.941C>T
  hgvsp: ENSP00000442718.1:p.Thr314Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.428C>T
  hgvsp: ENSP00000413132.2:p.Thr143Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.164C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1369C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.941C>T
  hgvsp: ENSP00000376230.2:p.Thr314Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.991C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.998C>T
  hgvsp: ENSP00000313422.5:p.Thr333Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*121C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.461C>T
  hgvsp: ENSP00000350532.4:p.Thr154Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.596C>T
  hgvsp: ENSP00000396723.2:p.Thr199Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.461C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.575C>T
  hgvsp: ENSP00000391598.2:p.Thr192Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1402C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.974C>T
  hgvsp: ENSP00000414847.2:p.Thr325Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5221C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.605C>T
  hgvsp: ENSP00000441406.1:p.Thr202Ile
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1385C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.971C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr333Ile
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

12-123467062-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467062
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467062
    reference: chr 12
allele count: 1
allele frequency: 8.320436656515735e-6
allele num: 120186
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.580G>C
  hgvsp: ENSP00000391598.2:p.Glu194Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1407G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.1003G>C
  hgvsp: ENSP00000313422.5:p.Glu335Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.466G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.466G>C
  hgvsp: ENSP00000350532.4:p.Glu156Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.946G>C
  hgvsp: ENSP00000376230.2:p.Glu316Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.577G>C
  hgvsp: ENSP00000406036.2:p.Glu193Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.979G>C
  hgvsp: ENSP00000414847.2:p.Glu327Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1374G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.169G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.433G>C
  hgvsp: ENSP00000413132.2:p.Glu145Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.601G>C
  hgvsp: ENSP00000396723.2:p.Glu201Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1390G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5226G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.996G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.976G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.610G>C
  hgvsp: ENSP00000396365.2:p.Glu204Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.610G>C
  hgvsp: ENSP00000441406.1:p.Glu204Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*126G>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.946G>C
  hgvsp: ENSP00000442718.1:p.Glu316Gln
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu335Gln
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP

12-123467065-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467065
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467065
    reference: chr 12
allele count: 7
allele frequency: 5.819753907549052e-5
allele num: 120280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.583C>T
  hgvsp: ENSP00000391598.2:p.Arg195Ter
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*129C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.580C>T
  hgvsp: ENSP00000406036.2:p.Arg194Ter
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1410C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.949C>T
  hgvsp: ENSP00000376230.2:p.Arg317Ter
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1393C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.982C>T
  hgvsp: ENSP00000414847.2:p.Arg328Ter
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.604C>T
  hgvsp: ENSP00000396723.2:p.Arg202Ter
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.172C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.613C>T
  hgvsp: ENSP00000441406.1:p.Arg205Ter
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.436C>T
  hgvsp: ENSP00000413132.2:p.Arg146Ter
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.613C>T
  hgvsp: ENSP00000396365.2:p.Arg205Ter
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5229C>T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.1006C>T
  hgvsp: ENSP00000313422.5:p.Arg336Ter
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1377C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.469C>T
  hgvsp: ENSP00000350532.4:p.Arg157Ter
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.979C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.999C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.949C>T
  hgvsp: ENSP00000442718.1:p.Arg317Ter
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.469C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg336Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

12-123467066-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467066
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467066
    reference: chr 12
allele count: 6
allele frequency: 4.986204833294552e-5
allele num: 120332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1411G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.605G>A
  hgvsp: ENSP00000396723.2:p.Arg202Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.470G>A
  hgvsp: ENSP00000350532.4:p.Arg157Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.470G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.1000G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.950G>A
  hgvsp: ENSP00000442718.1:p.Arg317Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.980G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.584G>A
  hgvsp: ENSP00000391598.2:p.Arg195Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*130G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5230G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1378G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.950G>A
  hgvsp: ENSP00000376230.2:p.Arg317Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.614G>A
  hgvsp: ENSP00000441406.1:p.Arg205Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.173G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.614G>A
  hgvsp: ENSP00000396365.2:p.Arg205Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.437G>A
  hgvsp: ENSP00000413132.2:p.Arg146Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.983G>A
  hgvsp: ENSP00000414847.2:p.Arg328Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1394G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.1007G>A
  hgvsp: ENSP00000313422.5:p.Arg336Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.581G>A
  hgvsp: ENSP00000406036.2:p.Arg194Gln
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg336Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum

12-123467066-GAC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467066
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467064
    reference: chr 12
allele count: 2
allele frequency: 1.662068277764851e-5
allele num: 120332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.618_619delCA
  hgvsp: ENSP00000396365.2:p.His206GlnfsTer?
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*134_*135delCA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.618_619delCA
  hgvsp: ENSP00000441406.1:p.His206GlnfsTer?
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.987_988delCA
  hgvsp: ENSP00000414847.2:p.His329GlnfsTer51
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.177_178delCA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.609_610delCA
  hgvsp: ENSP00000396723.2:p.His203GlnfsTer51
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5234_5235delCA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.474_475delCA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.585_586delCA
  hgvsp: ENSP00000406036.2:p.His195GlnfsTer51
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.474_475delCA
  hgvsp: ENSP00000350532.4:p.His158GlnfsTer?
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.1004_1005delCA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.441_442delCA
  hgvsp: ENSP00000413132.2:p.His147GlnfsTer51
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.588_589delCA
  hgvsp: ENSP00000391598.2:p.His196GlnfsTer?
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.954_955delCA
  hgvsp: ENSP00000442718.1:p.His318GlnfsTer51
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1382_1383delCA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1415_1416delCA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.954_955delCA
  hgvsp: ENSP00000376230.2:p.His318GlnfsTer?
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1398_1399delCA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.1011_1012delCA
  hgvsp: ENSP00000313422.5:p.His337GlnfsTer51
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.984_985delCA
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.His337GlnfsTer51
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: GAC
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

12-123467067-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467067
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467067
    reference: chr 12
allele count: 9
allele frequency: 7.477318799641089e-5
allele num: 120364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.615A>G
  hgvsp: ENST00000439686.2:c.615A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.438A>G
  hgvsp: ENST00000412505.2:c.438A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.471A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.174A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1412A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.951A>G
  hgvsp: ENST00000543566.1:c.951A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.1008A>G
  hgvsp: ENST00000315580.5:c.1008A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1395A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.951A>G
  hgvsp: ENST00000392435.2:c.951A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.606A>G
  hgvsp: ENST00000454885.2:c.606A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.471A>G
  hgvsp: ENST00000357866.4:c.471A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.984A>G
  hgvsp: ENST00000453766.2:c.984A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.615A>G
  hgvsp: ENST00000413381.2:c.615A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.1001A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.585A>G
  hgvsp: ENST00000456762.2:c.585A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1379A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.582A>G
  hgvsp: ENST00000426960.2:c.582A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5231A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.981A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*131A>G
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg336Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP

12-123467070-CAGAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467070
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467066
    reference: chr 12
allele count: 3
allele frequency: 2.489915840844579e-5
allele num: 120486
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.478_481delGAGA
  hgvsp: ENSP00000350532.4:p.Glu160SerfsTer?
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.991_994delGAGA
  hgvsp: ENSP00000414847.2:p.Glu331SerfsTer?
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1402_1405delGAGA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.1015_1018delGAGA
  hgvsp: ENSP00000313422.5:p.Glu339SerfsTer?
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.445_448delGAGA
  hgvsp: ENSP00000413132.2:p.Glu149SerfsTer?
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.958_961delGAGA
  hgvsp: ENSP00000442718.1:p.Glu320SerfsTer?
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.1008_1011delGAGA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.622_625delGAGA
  hgvsp: ENSP00000441406.1:p.Glu208SerfsTer?
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.988_991delGAGA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.589_592delGAGA
  hgvsp: ENSP00000406036.2:p.Glu197SerfsTer?
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.181_184delGAGA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.613_616delGAGA
  hgvsp: ENSP00000396723.2:p.Glu205SerfsTer?
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.958_961delGAGA
  hgvsp: ENSP00000376230.2:p.Glu320SerfsTer?
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.622_625delGAGA
  hgvsp: ENSP00000396365.2:p.Glu208SerfsTer?
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5238_5241delGAGA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.592_595delGAGA
  hgvsp: ENSP00000391598.2:p.Glu198SerfsTer?
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.478_481delGAGA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*138_*141delGAGA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1386_1389delGAGA
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1419_1422delGAGA
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu339SerfsTer?
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: CAGAG
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

12-123467070-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467070
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467070
    reference: chr 12
allele count: 1
allele frequency: 8.299719469481931e-6
allele num: 120486
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.441C>G
  hgvsp: ENSP00000413132.2:p.His147Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.588C>G
  hgvsp: ENSP00000391598.2:p.His196Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.609C>G
  hgvsp: ENSP00000396723.2:p.His203Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.1011C>G
  hgvsp: ENSP00000313422.5:p.His337Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.177C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.585C>G
  hgvsp: ENSP00000406036.2:p.His195Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.618C>G
  hgvsp: ENSP00000441406.1:p.His206Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1382C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.618C>G
  hgvsp: ENSP00000396365.2:p.His206Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.474C>G
  hgvsp: ENSP00000350532.4:p.His158Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.984C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*134C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1398C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.987C>G
  hgvsp: ENSP00000414847.2:p.His329Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.954C>G
  hgvsp: ENSP00000442718.1:p.His318Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.954C>G
  hgvsp: ENSP00000376230.2:p.His318Gln
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5234C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1415C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.474C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.1004C>G
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.His337Gln
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

12-123467072-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467072
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467072
    reference: chr 12
allele count: 1
allele frequency: 8.29655195300833e-6
allele num: 120532
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.620G>A
  hgvsp: ENSP00000441406.1:p.Arg207Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.1013G>A
  hgvsp: ENSP00000313422.5:p.Arg338Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.956G>A
  hgvsp: ENSP00000376230.2:p.Arg319Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5236G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1417G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.476G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.476G>A
  hgvsp: ENSP00000350532.4:p.Arg159Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.611G>A
  hgvsp: ENSP00000396723.2:p.Arg204Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.956G>A
  hgvsp: ENSP00000442718.1:p.Arg319Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.989G>A
  hgvsp: ENSP00000414847.2:p.Arg330Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.443G>A
  hgvsp: ENSP00000413132.2:p.Arg148Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.587G>A
  hgvsp: ENSP00000406036.2:p.Arg196Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.620G>A
  hgvsp: ENSP00000396365.2:p.Arg207Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.986G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.179G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.590G>A
  hgvsp: ENSP00000391598.2:p.Arg197Lys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*136G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1400G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1384G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.1006G>A
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg338Lys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

12-123467076-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467076
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467076
    reference: chr 12
allele count: 5
allele frequency: 4.145730726497852e-5
allele num: 120606
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.183G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.1017G>A
  hgvsp: ENST00000315580.5:c.1017G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.615G>A
  hgvsp: ENST00000454885.2:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5240G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.591G>A
  hgvsp: ENST00000426960.2:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.480G>A
  hgvsp: ENST00000357866.4:c.480G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.594G>A
  hgvsp: ENST00000456762.2:c.594G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1388G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.480G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.447G>A
  hgvsp: ENST00000412505.2:c.447G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.624G>A
  hgvsp: ENST00000439686.2:c.624G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.960G>A
  hgvsp: ENST00000543566.1:c.960G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1421G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.960G>A
  hgvsp: ENST00000392435.2:c.960G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.990G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.1010G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.993G>A
  hgvsp: ENST00000453766.2:c.993G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*140G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.624G>A
  hgvsp: ENST00000413381.2:c.624G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1404G>A
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu339Glu
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/12-123467080-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467080
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467080
    reference: chr 12
allele count: 1
allele frequency: 8.289124668435012e-6
allele num: 120640
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.994A>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.1021A>C
  hgvsp: ENSP00000313422.5:p.Asn341His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1392A>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.451A>C
  hgvsp: ENSP00000413132.2:p.Asn151His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1425A>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1408A>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.619A>C
  hgvsp: ENSP00000396723.2:p.Asn207His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5244A>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.628A>C
  hgvsp: ENSP00000396365.2:p.Asn210His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.598A>C
  hgvsp: ENSP00000391598.2:p.Asn200His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.628A>C
  hgvsp: ENSP00000441406.1:p.Asn210His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.964A>C
  hgvsp: ENSP00000376230.2:p.Asn322His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.964A>C
  hgvsp: ENSP00000442718.1:p.Asn322His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.484A>C
  hgvsp: ENSP00000350532.4:p.Asn162His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.1014A>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*144A>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.997A>C
  hgvsp: ENSP00000414847.2:p.Asn333His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.595A>C
  hgvsp: ENSP00000406036.2:p.Asn199His
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.484A>C
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.187A>C
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn341His
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

12-123467083-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467083
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467083
    reference: chr 12
allele count: 3
allele frequency: 2.485707183693761e-5
allele num: 120690
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.967A>G
  hgvsp: ENSP00000376230.2:p.Lys323Glu
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.1024A>G
  hgvsp: ENSP00000313422.5:p.Lys342Glu
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5247A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.598A>G
  hgvsp: ENSP00000406036.2:p.Lys200Glu
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.1000A>G
  hgvsp: ENSP00000414847.2:p.Lys334Glu
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.631A>G
  hgvsp: ENSP00000396365.2:p.Lys211Glu
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*147A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000441406
  ensembl transcript: ENST00000413381
  gene symbol: ARL6IP4
  hgvsc: ENST00000413381.2:c.631A>G
  hgvsp: ENSP00000441406.1:p.Lys211Glu
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.487A>G
  hgvsp: ENSP00000350532.4:p.Lys163Glu
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.967A>G
  hgvsp: ENSP00000442718.1:p.Lys323Glu
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.487A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1411A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.190A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.622A>G
  hgvsp: ENSP00000396723.2:p.Lys208Glu
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1395A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.1017A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1428A>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.601A>G
  hgvsp: ENSP00000391598.2:p.Lys201Glu
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.997A>G
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys342Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ

12-123467085-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467085
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467085
    reference: chr 12
allele count: 1
allele frequency: 8.283906027370025e-6
allele num: 120716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1413G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.969G>A
  hgvsp: ENST00000543566.1:c.969G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.489G>A
  hgvsp: ENST00000357866.4:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.624G>A
  hgvsp: ENST00000454885.2:c.624G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.969G>A
  hgvsp: ENST00000392435.2:c.969G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.1002G>A
  hgvsp: ENST00000453766.2:c.1002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.192G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*149G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1397G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.600G>A
  hgvsp: ENST00000426960.2:c.600G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.1026G>A
  hgvsp: ENST00000315580.5:c.1026G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1430G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.603G>A
  hgvsp: ENST00000456762.2:c.603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.999G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5249G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.1019G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.489G>A
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.633G>A
  hgvsp: ENST00000439686.2:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.456G>A
  hgvsp: ENST00000412505.2:c.456G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18076
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.1026G>A
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

12-123467095-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467095
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467095
    reference: chr 12
allele count: 1
allele frequency: 8.277734549608463e-6
allele num: 120806
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.600+10G>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.1019+10G>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.633+10G>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.1002+10G>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.1009G>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*149+10G>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.202G>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.499G>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.489+10G>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.624+10G>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1397+10G>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.613G>T
  hgvsp: ENSP00000391598.2:p.Ala205Ser
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1440G>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1413+10G>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.979G>T
  hgvsp: ENSP00000376230.2:p.Ala327Ser
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.456+10G>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.969+10G>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.1026+10G>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5259G>T
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala327Ser
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

12-123467104-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467104
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467104
    reference: chr 12
allele count: 1
allele frequency: 8.274720728175424e-6
allele num: 120850
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.508C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.1018C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.1019+19C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.489+19C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1397+19C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.600+19C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.211C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*149+19C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5268C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1449C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.622C>T
  hgvsp: ENSP00000391598.2:p.Pro208Ser
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.456+19C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.988C>T
  hgvsp: ENSP00000376230.2:p.Pro330Ser
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.624+19C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.1002+19C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1413+19C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.1026+19C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.633+19C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.969+19C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro330Ser
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

12-123467112-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467112
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467112
    reference: chr 12
allele count: 1
allele frequency: 8.273625337150233e-6
allele num: 120866
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.630C>G
  hgvsp: ENSP00000391598.2:p.Ile210Met
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540382
  gene symbol: ARL6IP4
  hgvsc: ENST00000540382.1:n.1413+27C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000406036
  ensembl transcript: ENST00000426960
  gene symbol: ARL6IP4
  hgvsc: ENST00000426960.2:c.600+27C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.996C>G
  hgvsp: ENSP00000376230.2:p.Ile332Met
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.1026C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000350532
  ensembl transcript: ENST00000357866
  gene symbol: ARL6IP4
  hgvsc: ENST00000357866.4:c.489+27C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000313422
  ensembl transcript: ENST00000315580
  gene symbol: ARL6IP4
  hgvsc: ENST00000315580.5:c.1026+27C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.516C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000256028
  ensembl transcript: ENST00000540866
  gene symbol: RP11-197N18.2
  hgvsc: ENST00000540866.2:n.5276C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000413132
  ensembl transcript: ENST00000412505
  gene symbol: ARL6IP4
  hgvsc: ENST00000412505.2:c.456+27C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.969+27C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000539576
  gene symbol: ARL6IP4
  hgvsc: ENST00000539576.1:n.1397+27C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.624+27C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.1019+27C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.1002+27C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.219C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000540708
  gene symbol: ARL6IP4
  hgvsc: ENST00000540708.1:n.1457C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.633+27C>G
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*149+27C>G
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile332Met
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

12-123467113-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 123467113
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 123467113
    reference: chr 12
allele count: 4
allele frequency: 3.309395373465268e-5
allele num: 120868
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396723
  ensembl transcript: ENST00000454885
  gene symbol: ARL6IP4
  hgvsc: ENST00000454885.2:c.624+28C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000442210
  gene symbol: ARL6IP4
  hgvsc: ENST00000442210.2:n.517C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000442718
  ensembl transcript: ENST00000543566
  gene symbol: ARL6IP4
  hgvsc: ENST00000543566.1:c.969+28C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000414847
  ensembl transcript: ENST00000453766
  gene symbol: ARL6IP4
  hgvsc: ENST00000453766.2:c.1002+28C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536073
  gene symbol: ARL6IP4
  hgvsc: ENST00000536073.1:n.220C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000392433
  gene symbol: ARL6IP4
  hgvsc: ENST00000392433.3:n.1027C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000391598
  ensembl transcript: ENST00000456762
  gene symbol: ARL6IP4
  hgvsc: ENST00000456762.2:c.631C>T
  hgvsp: ENSP00000391598.2:p.Arg211Cys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000376230
  ensembl transcript: ENST00000392435
  gene symbol: ARL6IP4
  hgvsc: ENST00000392435.2:c.997C>T
  hgvsp: ENSP00000376230.2:p.Arg333Cys
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000396365
  ensembl transcript: ENST00000439686
  gene symbol: ARL6IP4
  hgvsc: ENST00000439686.2:c.633+28C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl transcript: ENST00000536502
  gene symbol: ARL6IP4
  hgvsc: ENST00000536502.1:n.1019+28C>T
  variant of: http://identifiers.org/hgnc/18076
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182196
  ensembl protein: ENSP00000438969
  ensembl transcript: ENST00000539770
  gene symbol: ARL6IP4
  hgvsc: ENST00000539770.1:c.*149+28C>T
  variant of: http://identifiers.org/hgnc/18076
canonical: false
consequence: missense
filter: PASS
hgvs: p.Arg333Cys
num of homozygotes: 0
reference allele: C

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000182196
ensembl transcript: ENST00000540708
gene symbol: ARL6IP4
hgvsc: ENST00000540708.1:n.951A>C
variant of: http://identifiers.org/hgnc/18076

GenotypeDepth
all individuals: 36656
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 774
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 322
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5852
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14604
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1025
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 156
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 740
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 6.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7587
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1107
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3345
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 740
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3033
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40400
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.584772442461106e-5
allele num: 65434
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.83e-1

QD
type: SiteQuality
SIO_000300: 1.217e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 1.464587e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000182196
ensembl protein: ENSP00000391598
ensembl transcript: ENST00000456762
gene symbol: ARL6IP4
hgvsc: ENST00000456762.2:c.519G>C
hgvsp: ENSP00000391598.2:p.Glu173Asp
variant of: http://identifiers.org/hgnc/18076

GenotypeDepth
all individuals: 158
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14605
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 772
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5856
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36648
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1027
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3346
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 653
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3031
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1112
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7586
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40419
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65428
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10114
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.078288353999514e-5
allele num: 16452
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.464555e6

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 5.245e0

MQRankSum
type: SiteQuality
SIO_000300: 4.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.19e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e0

QD
type: SiteQuality
SIO_000300: 1.35e1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000182196
ensembl protein: ENSP00000442200
ensembl transcript: ENST00000542099
gene symbol: ARL6IP4
hgvsc: ENST00000542099.1:c.911C>T
hgvsp: ENSP00000442200.1:p.Thr304Met
variant of: http://identifiers.org/hgnc/18076

GenotypeDepth
all individuals: 123
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 162
bin: 2.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36606
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5866
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 337
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 762
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 786
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 14582
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1029
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2032
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1127
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 205
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3343
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 665
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7577
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40305
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3031
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10110
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.131221719457014e-3
allele num: 884
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.89e-1

FS
type: SiteQuality
SIO_000300: 9.429999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e0

MQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

QD
type: SiteQuality
SIO_000300: 1.604e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.19e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.49e-1

DP
type: SiteQuality
SIO_000300: 1.463981e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000182196
ensembl transcript: ENST00000540708
gene symbol: ARL6IP4
hgvsc: ENST00000540708.1:n.959C>T
variant of: http://identifiers.org/hgnc/18076

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

GenotypeDepth
all individuals: 812
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14539
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36603
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1023
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 798
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5860
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 167
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 326
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 654
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 170
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3032
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40323
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7572
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1177
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 741
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3337
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2032
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529940944279551e-5
allele num: 65362
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.551e0

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.347e1

DP
type: SiteQuality
SIO_000300: 1.462976e6

VQSLOD
type: SiteQuality
SIO_000300: 3.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.74e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000182196
ensembl transcript: ENST00000539576
gene symbol: ARL6IP4
hgvsc: ENST00000539576.1:n.927G>A
variant of: http://identifiers.org/hgnc/18076

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 338
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 821
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 814
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14531
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 25
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 36568
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 16
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5847
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 326
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 124
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 9.75e1
variant carriers: 5

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

GenotypeQuality
all individuals: 207
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40250
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3030
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2034
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3335
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7566
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 1171
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 8
allele frequency: 9.313154831199069e-4
allele num: 8590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10096
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.061474406073965e-5
allele num: 65328
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.14e-1

FS
type: SiteQuality
SIO_000300: 2.474e0

DP
type: SiteQuality
SIO_000300: 1.462996e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 3.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.47e-1

QD
type: SiteQuality
SIO_000300: 1.174e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000182196
ensembl transcript: ENST00000536502
gene symbol: ARL6IP4
hgvsc: ENST00000536502.1:n.945A>G
variant of: http://identifiers.org/hgnc/18076

GenotypeDepth
all individuals: 324
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 828
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 36561
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 843
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5829
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14541
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 8.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 1025
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40286
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7581
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2035
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3030
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3340
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 8.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10088
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530924678505817e-5
allele num: 65320
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.91e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.462274e6

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

QD
type: SiteQuality
SIO_000300: 1.349e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
ensembl gene: ENSG00000182196
ensembl protein: ENSP00000391598
ensembl transcript: ENST00000456762
gene symbol: ARL6IP4
hgvsc: ENST00000456762.2:c.533G>C
hgvsp: ENSP00000391598.2:p.Arg178Thr
variant of: http://identifiers.org/hgnc/18076

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000182196
ensembl transcript: ENST00000540708
gene symbol: ARL6IP4
hgvsc: ENST00000540708.1:n.966G>C
variant of: http://identifiers.org/hgnc/18076

GenotypeDepth
all individuals: 5836
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36470
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14502
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1027
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 882
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 363
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 841
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 327
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3027
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1238
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 657
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3336
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7576
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2036
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40192
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.987676406281057e-4
allele num: 10062
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.429999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.79e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.096e1

FS
type: SiteQuality
SIO_000300: 2.701e0

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.52e-1

DP
type: SiteQuality
SIO_000300: 1.461067e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000182196
ensembl transcript: ENST00000392433
gene symbol: ARL6IP4
hgvsc: ENST00000392433.3:n.929+6G>A
variant of: http://identifiers.org/hgnc/18076

GenotypeDepth
all individuals: 16
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1029
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 218
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 884
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 36299
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 394
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5838
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 328
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14452
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 994
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 187
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39927
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3027
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2040
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1298
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 678
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7554
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3337
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533789380042332e-5
allele num: 65198
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10026
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.458343e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.211e0

QD
type: SiteQuality
SIO_000300: 9.050000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: -2.078e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

GenotypeDepth
all individuals: 903
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14390
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36180
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5841
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 243
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1077
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 328
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 128
bin: 4.75e1
variant carriers: 2

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

GenotypeDepth
all individuals: 1036
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39738
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3338
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7541
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 219
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2036
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3027
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.329916123019571e-4
allele num: 8584
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10000
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.606596646397641e-5
allele num: 65124
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

FS
type: SiteQuality
SIO_000300: 2.527e0

QD
type: SiteQuality
SIO_000300: 1.053e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

DP
type: SiteQuality
SIO_000300: 1.456435e6

VQSLOD
type: SiteQuality
SIO_000300: 8.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.15e-1

GenotypeDepth
all individuals: 243
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36161
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1097
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 438
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14385
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 907
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1036
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5831
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 126
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3334
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 64
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1328
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7530
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39672
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 125
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2039
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3022
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.084945843981989e-5
allele num: 16434
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.535720867375146e-5
allele num: 65116
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9988
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.83e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.146e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.83e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.206e0

DP
type: SiteQuality
SIO_000300: 1.456134e6

QD
type: SiteQuality
SIO_000300: 1.142e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

GenotypeDepth
all individuals: 36014
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 912
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5830
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1036
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 327
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1202
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14316
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 6.25e1
variant carriers: 2

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

GenotypeDepth
all individuals: 525
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 747
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7532
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39569
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1338
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2038
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3025
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 97
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3337
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 657
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65082
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9988
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.329373398555789e-4
allele num: 8586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

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

GenotypeDepth
all individuals: 22013
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2477
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5333
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2855
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 345
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2794
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1065
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1519
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1150
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22144
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20081
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3159
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1007
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6674
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5628
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.954183900731785e-5
allele num: 12572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4954
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.477823479855295e-5
allele num: 40358
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.44e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.84256e5

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.144e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.934e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000182196
ensembl protein: ENSP00000406036
ensembl transcript: ENST00000426960
gene symbol: ARL6IP4
hgvsc: ENST00000426960.2:c.531-6C>T
variant of: http://identifiers.org/hgnc/18076

GenotypeDepth
all individuals: 22631
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2657
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18977
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 694
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6119
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 848
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6093
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 344
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2015
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 12
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19207
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 268
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2425
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1228
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1468
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1120
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2481
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23403
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3586
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13054
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.25032629731311e-5
allele num: 44438
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7150
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3976
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.905e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.223e0

VQSLOD
type: SiteQuality
SIO_000300: -1.04e0

QD
type: SiteQuality
SIO_000300: 1.06e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.049541e6

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000182196
ensembl protein: ENSP00000396365
ensembl transcript: ENST00000439686
gene symbol: ARL6IP4
hgvsc: ENST00000439686.2:c.564-3C>T
variant of: http://identifiers.org/hgnc/18076

GenotypeDepth
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6643
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 859
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 584
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16876
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2782
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5489
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24863
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 344
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1943
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 125
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3871
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2163
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2248
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26014
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 153
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17187
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 721
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 739
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1350
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.347057081200017e-5
allele num: 47266
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4216
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7454
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5900
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

DP
type: SiteQuality
SIO_000300: 1.092133e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.695e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000182196
ensembl transcript: ENST00000392433
gene symbol: ARL6IP4
hgvsc: ENST00000392433.3:n.931C>T
variant of: http://identifiers.org/hgnc/18076

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000182196
ensembl transcript: ENST00000539576
gene symbol: ARL6IP4
hgvsc: ENST00000539576.1:n.1329C>T
variant of: http://identifiers.org/hgnc/18076

GenotypeDepth
all individuals: 870
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28341
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1674
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 9
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2902
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13945
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4553
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 439
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 7317
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1427
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14297
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4220
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 156
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1734
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1871
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29944
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 287
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7874
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50750
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4556
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.171395483497394e-4
allele num: 13816
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 670
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7974
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.08e-1

FS
type: SiteQuality
SIO_000300: 7.63e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.733e0

QD
type: SiteQuality
SIO_000300: 1.35e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.72e-1

DP
type: SiteQuality
SIO_000300: 1.152233e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.149999999999999e-1

GenotypeDepth
all individuals: 9
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3978
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1382
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30690
bin: 2.25e1
variant carriers: 3

GenotypeDepth
all individuals: 127
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 18
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7583
bin: 2.75e1
variant carriers: 4

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 872
bin: 3.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 12197
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2964
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 346
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1313
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4442
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1008
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12548
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 411
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1626
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1479
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32506
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.510859301227573e-4
allele num: 52950
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 700
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14054
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.229105211406096e-4
allele num: 8136
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4776
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.18638e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.23e-1

ClippingRankSum
type: SiteQuality
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BaseQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Latino
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South Asian
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African
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MQ
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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ClippingRankSum
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MQ
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VQSLOD
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BaseQRankSum
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DP
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FS
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QD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Non-Finnish)
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African
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East Asian
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FS
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ReadPosRankSum
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VQSLOD
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MQRankSum
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DP
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GenotypeQuality
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African
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East Asian
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VQSLOD
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QD
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DP
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FS
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MQ
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Latino
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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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European (Non-Finnish)
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ReadPosRankSum
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DP
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QD
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MQ
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.532379171902295e-5
allele num: 65258
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.04905936518584e-5
allele num: 65594
num of homozygotes: 0

East Asian
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allele frequency: 3.481894150417827e-4
allele num: 8616
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African
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South Asian
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allele frequency: 0.0e0
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Other
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European (Finnish)
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Latino
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VQSLOD
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SIO_000300: 5.59e0

ClippingRankSum
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BaseQRankSum
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MQ
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MQRankSum
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FS
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DP
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QD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
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European (Finnish)
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African
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num of homozygotes: 0

Latino
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Other
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South Asian
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East Asian
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ClippingRankSum
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InbreedingCoeff
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QD
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VQSLOD
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MQRankSum
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MQ
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ReadPosRankSum
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FS
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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Other
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East Asian
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European (Non-Finnish)
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DP
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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FS
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MQRankSum
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MQ
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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South Asian
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Other
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European (Finnish)
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Latino
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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MQ
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InbreedingCoeff
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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QD
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DP
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MQ
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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African
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European (Non-Finnish)
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Other
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QD
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FS
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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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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MQ
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BaseQRankSum
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DP
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MQRankSum
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FS
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QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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East Asian
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European (Non-Finnish)
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BaseQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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QD
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South Asian
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European (Non-Finnish)
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African
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European (Finnish)
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East Asian
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FS
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MQ
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QD
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DP
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SIO_000300: 1.451e6

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.16e-1

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

GenotypeDepth
all individuals: 18
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 400
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1003
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4505
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 41324
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12577
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 128
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6376
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1794
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.521606816798539e-4
allele num: 6572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66070
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.93e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.16e-1

FS
type: SiteQuality
SIO_000300: 3.387e0

DP
type: SiteQuality
SIO_000300: 1.451e6

QD
type: SiteQuality
SIO_000300: 1.297e1

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.67e-1

GenotypeDepth
all individuals: 12
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 41315
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4517
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 128
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12597
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1004
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 385
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1965
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variant carriers: 0

GenotypeQuality
all individuals: 47405
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1796
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6371
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66102
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

MQ
type: SiteQuality
SIO_000300: 5.918e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.618e0

VQSLOD
type: SiteQuality
SIO_000300: -8.016e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.185e0

FS
type: SiteQuality
SIO_000300: 5.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.254e0

DP
type: SiteQuality
SIO_000300: 1.451678e6

QD
type: SiteQuality
SIO_000300: 9.869999999999999e0

GenotypeDepth
all individuals: 13
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 131
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variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 18
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 41306
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12643
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4518
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 999
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variant carriers: 0

GenotypeQuality
all individuals: 1069
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variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47454
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6380
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 370
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.62962962962963e-4
allele num: 8640
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512172992590352e-5
allele num: 66130
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.75e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

MQRankSum
type: SiteQuality
SIO_000300: 4.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

DP
type: SiteQuality
SIO_000300: 1.452601e6

QD
type: SiteQuality
SIO_000300: 1.155e1

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.28e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.05e0

GenotypeDepth
all individuals: 20
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 18
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 41313
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 128
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 334
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4521
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 101
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 999
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 44
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12678
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variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
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variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6389
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1801
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variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1072
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1964
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47498
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66150
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.067961165048543e-5
allele num: 16480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.089e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.179e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.95e-1

FS
type: SiteQuality
SIO_000300: 1.0717e1

DP
type: SiteQuality
SIO_000300: 1.45331e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
ensembl gene: ENSG00000182196
ensembl protein: ENSP00000413132
ensembl transcript: ENST00000412505
gene symbol: ARL6IP4
hgvsc: ENST00000412505.2:c.454A>G
hgvsp: ENSP00000413132.2:p.Lys152Glu
variant of: http://identifiers.org/hgnc/18076

GenotypeDepth
all individuals: 12693
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1004
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 41329
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 94
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 371
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 310
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 13
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 128
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 19
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4521
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6397
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47523
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 370
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1800
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66184
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.819725827975252e-4
allele num: 16486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.56e-1

FS
type: SiteQuality
SIO_000300: 4.056e0

DP
type: SiteQuality
SIO_000300: 1.453933e6

QD
type: SiteQuality
SIO_000300: 1.015e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000182196
ensembl protein: ENSP00000441406
ensembl transcript: ENST00000413381
gene symbol: ARL6IP4
hgvsc: ENST00000413381.2:c.633G>A
hgvsp: ENST00000413381.2:c.633G>A(p.%3D)
variant of: http://identifiers.org/hgnc/18076

GenotypeDepth
all individuals: 4530
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12705
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 371
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 301
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1000
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 128
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 41318
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47523
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6399
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1802
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510619656182966e-5
allele num: 66198
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -3.57e-1

FS
type: SiteQuality
SIO_000300: 5.659999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.454132e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

VQSLOD
type: SiteQuality
SIO_000300: -3.32e-2

QD
type: SiteQuality
SIO_000300: 1.2e1

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1006
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12768
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 41287
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 129
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 266
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4538
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 374
bin: 4.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6410
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47557
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66252
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.57e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.18e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.078e0

QD
type: SiteQuality
SIO_000300: 5.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.81e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

DP
type: SiteQuality
SIO_000300: 1.455338e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 128
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 250
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 41278
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 12803
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4549
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 372
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 269
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1810
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47607
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6418
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508705229172324e-5
allele num: 66282
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.77e-1

DP
type: SiteQuality
SIO_000300: 1.456014e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.796e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

QD
type: SiteQuality
SIO_000300: 1.157e1

VQSLOD
type: SiteQuality
SIO_000300: 2.52e-1

GenotypeDepth
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 86
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1005
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4565
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12822
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 5.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47581
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1070
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6425
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1972
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508523155830442e-5
allele num: 66290
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 2.535e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.068e0

QD
type: SiteQuality
SIO_000300: 1.87e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.137e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.63e-1

DP
type: SiteQuality
SIO_000300: 1.456457e6