14-105963772-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105963772
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105963772
    reference: chr 14
allele count: 2
allele frequency: 9.493070058857034e-5
allele num: 21068
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.763C>T
  hgvsp: ENSP00000376307.3:p.Arg255Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3282C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.229C>T
  hgvsp: ENSP00000391436.1:p.Arg77Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.541C>T
  hgvsp: ENSP00000376312.1:p.Arg181Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000399624
  ensembl transcript: ENST00000455454
  gene symbol: C14orf80
  hgvsc: ENST00000455454.1:c.640C>T
  hgvsp: ENSP00000399624.1:p.Arg214Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.640C>T
  hgvsp: ENSP00000400604.1:p.Arg214Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.970C>T
  hgvsp: ENSP00000376308.4:p.Arg324Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.547C>T
  hgvsp: ENSP00000333010.7:p.Arg183Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.385C>T
  hgvsp: ENSP00000400014.1:p.Arg129Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546536
  gene symbol: C14orf80
  hgvsc: ENST00000546536.1:n.867C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.718C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.664C>T
  hgvsp: ENSP00000346568.6:p.Arg222Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*189C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.541C>T
  hgvsp: ENSP00000333959.7:p.Arg181Trp
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34155
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg255Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

14-105963773-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105963773
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105963773
    reference: chr 14
allele count: 1
allele frequency: 4.749691270067446e-5
allele num: 21054
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.764G>A
  hgvsp: ENSP00000376307.3:p.Arg255Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.641G>A
  hgvsp: ENSP00000400604.1:p.Arg214Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.542G>A
  hgvsp: ENSP00000376312.1:p.Arg181Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000399624
  ensembl transcript: ENST00000455454
  gene symbol: C14orf80
  hgvsc: ENST00000455454.1:c.641G>A
  hgvsp: ENSP00000399624.1:p.Arg214Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.386G>A
  hgvsp: ENSP00000400014.1:p.Arg129Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.719G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546536
  gene symbol: C14orf80
  hgvsc: ENST00000546536.1:n.868G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.548G>A
  hgvsp: ENSP00000333010.7:p.Arg183Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.665G>A
  hgvsp: ENSP00000346568.6:p.Arg222Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.971G>A
  hgvsp: ENSP00000376308.4:p.Arg324Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.230G>A
  hgvsp: ENSP00000391436.1:p.Arg77Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.542G>A
  hgvsp: ENSP00000333959.7:p.Arg181Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3283G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*190G>A
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6993
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg255Gln
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

14-105963792-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105963792
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105963792
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 20650
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.726+12C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*197+12C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.672+12C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.978+12C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.237+12C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.771+12C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3302C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.549+12C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.393+12C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546536
  gene symbol: C14orf80
  hgvsc: ENST00000546536.1:n.887C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.648+12C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.555+12C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.549+12C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32893
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3451
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD

14-105963794-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105963794
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105963794
    reference: chr 14
allele count: 102
allele frequency: 4.952417945232084e-3
allele num: 20596
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.549+14C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.549+14C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3304C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.648+14C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.978+14C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.555+14C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546536
  gene symbol: C14orf80
  hgvsc: ENST00000546536.1:n.889C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.393+14C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.672+14C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.726+14C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.771+14C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*197+14C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.237+14C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32686
  bin: 2.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 7.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 3.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-105963795-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105963795
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105963795
    reference: chr 14
allele count: 1
allele frequency: 4.855783237836263e-5
allele num: 20594
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3305G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*197+15G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.549+15G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.771+15G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.648+15G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.726+15G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.672+15G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.978+15G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.555+15G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546536
  gene symbol: C14orf80
  hgvsc: ENST00000546536.1:n.890G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.549+15G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.237+15G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.393+15G>A
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

14-105963795-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105963795
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105963795
    reference: chr 14
allele count: 1
allele frequency: 4.855783237836263e-5
allele num: 20594
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3305G>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.237+15G>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.726+15G>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.672+15G>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.549+15G>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.555+15G>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.393+15G>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546536
  gene symbol: C14orf80
  hgvsc: ENST00000546536.1:n.890G>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.771+15G>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.648+15G>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.978+15G>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.549+15G>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*197+15G>C
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

14-105963795-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105963795
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105963795
    reference: chr 14
allele count: 2
allele frequency: 9.711566475672526e-5
allele num: 20594
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.555+15G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*197+15G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3305G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.549+15G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.549+15G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.726+15G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546536
  gene symbol: C14orf80
  hgvsc: ENST00000546536.1:n.890G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.237+15G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.978+15G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.648+15G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.393+15G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.672+15G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.771+15G>T
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-105963806-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105963806
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105963806
    reference: chr 14
allele count: 3
allele frequency: 1.463414634146341e-4
allele num: 20500
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546536
  gene symbol: C14orf80
  hgvsc: ENST00000546536.1:n.901C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3316C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.549+26C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.648+26C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.726+26C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.978+26C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*197+26C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.237+26C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.771+26C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.672+26C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.549+26C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.393+26C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.555+26C>G
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30873
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

14-105963806-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105963806
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105963806
    reference: chr 14
allele count: 1
allele frequency: 4.878048780487805e-5
allele num: 20500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3316C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.978+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.237+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.726+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.555+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546536
  gene symbol: C14orf80
  hgvsc: ENST00000546536.1:n.901C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.393+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.672+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.771+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.549+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.549+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*197+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.648+26C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30873
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum

14-105963807-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105963807
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105963807
    reference: chr 14
allele count: 4
allele frequency: 1.953697372277034e-4
allele num: 20474
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.978+27C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546536
  gene symbol: C14orf80
  hgvsc: ENST00000546536.1:n.902C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.549+27C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.393+27C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.726+27C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.237+27C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3317C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.549+27C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*197+27C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.648+27C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.555+27C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.771+27C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.672+27C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30768
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

14-105963820-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105963820
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105963820
    reference: chr 14
allele count: 1
allele frequency: 4.909180166912126e-5
allele num: 20370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.549+40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.771+40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546536
  gene symbol: C14orf80
  hgvsc: ENST00000546536.1:n.915C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3330C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.237+40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.726+40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.978+40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.393+40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*197+40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.555+40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.549+40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.648+40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.672+40C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29274
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-105963829-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105963829
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105963829
    reference: chr 14
allele count: 1
allele frequency: 4.922713399625874e-5
allele num: 20314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3339C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.771+49C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.978+49C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.648+49C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.549+49C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.549+49C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.672+49C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*197+49C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.555+49C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546536
  gene symbol: C14orf80
  hgvsc: ENST00000546536.1:n.924C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.726+49C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.237+49C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.393+49C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29197
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

14-105964085-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964085
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964085
    reference: chr 14
allele count: 2
allele frequency: 1.613163413453783e-4
allele num: 12398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.550-50C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*198-50C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.238-50C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.550-50C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.727-50C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3595C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.673-50C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.394-50C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.649-50C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.123C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.772-50C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.556-50C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.979-50C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22266
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29296
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-105964088-T-TCTGTCCCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964088
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964096
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 12460
alternate allele: TCTGTCCCC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.127_134dupCTGTCCCC
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22341
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3096
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29344
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

14-105964095-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964095
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964095
    reference: chr 14
allele count: 3
allele frequency: 2.378686964795433e-4
allele num: 12612
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.979-40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3605C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.727-40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.133C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.673-40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*198-40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.394-40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.238-40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.550-40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.772-40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.550-40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.556-40C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.649-40C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28455
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23351
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

14-105964103-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964103
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964103
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 12984
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.141T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.238-32T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.649-32T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.673-32T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.550-32T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.550-32T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.772-32T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3613T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.979-32T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.556-32T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*198-32T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.394-32T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.727-32T>C
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25733
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

14-105964110-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964110
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964110
    reference: chr 14
allele count: 2
allele frequency: 1.454545454545455e-4
allele num: 13750
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.238-25C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.394-25C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3620C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*198-25C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.649-25C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.148C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.550-25C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.550-25C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.673-25C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.979-25C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.772-25C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.556-25C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.727-25C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3662
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27790
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23873
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

14-105964111-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964111
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964111
    reference: chr 14
allele count: 1
allele frequency: 7.174630506528914e-5
allele num: 13938
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*198-24G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.673-24G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.550-24G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.979-24G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3621G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.550-24G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.727-24G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.394-24G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.238-24G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.772-24G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.149G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.556-24G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.649-24G>A
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28486
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

14-105964115-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964115
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964115
    reference: chr 14
allele count: 1
allele frequency: 6.838074398249453e-5
allele num: 14624
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.649-20T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.979-20T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.153T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.772-20T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.727-20T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3625T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.238-20T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.550-20T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*198-20T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.550-20T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.394-20T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.673-20T>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.556-20T>C
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21477
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

14-105964125-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964125
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964125
    reference: chr 14
allele count: 1
allele frequency: 6.337135614702154e-5
allele num: 15780
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.772-10G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3635G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.979-10G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.550-10G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.163G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.550-10G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.238-10G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.394-10G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*198-10G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.556-10G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.673-10G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.727-10G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.649-10G>T
  variant of: http://identifiers.org/hgnc/20127
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18602
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32583
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

14-105964139-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964139
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964139
    reference: chr 14
allele count: 4
allele frequency: 2.26295541977823e-4
allele num: 17676
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.242C>T
  hgvsp: ENSP00000391436.1:p.Thr81Met
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.653C>T
  hgvsp: ENSP00000400604.1:p.Thr218Met
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.983C>T
  hgvsp: ENSP00000376308.4:p.Thr328Met
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.677C>T
  hgvsp: ENSP00000346568.6:p.Thr226Met
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.776C>T
  hgvsp: ENSP00000376307.3:p.Thr259Met
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*202C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.398C>T
  hgvsp: ENSP00000400014.1:p.Thr133Met
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.731C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.177C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.554C>T
  hgvsp: ENSP00000376312.1:p.Thr185Met
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.560C>T
  hgvsp: ENSP00000333010.7:p.Thr187Met
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.554C>T
  hgvsp: ENSP00000333959.7:p.Thr185Met
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3649C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15514
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34656
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr259Met
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

14-105964140-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964140
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964140
    reference: chr 14
allele count: 1
allele frequency: 5.471656817684395e-5
allele num: 18276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.555G>A
  hgvsp: ENST00000392527.1:c.555G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.984G>A
  hgvsp: ENST00000392523.4:c.984G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.399G>A
  hgvsp: ENST00000421892.1:c.399G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.561G>A
  hgvsp: ENST00000329886.7:c.561G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.678G>A
  hgvsp: ENST00000354560.6:c.678G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*203G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.243G>A
  hgvsp: ENST00000450383.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.654G>A
  hgvsp: ENST00000432805.1:c.654G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.732G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.777G>A
  hgvsp: ENST00000392522.3:c.777G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.555G>A
  hgvsp: ENST00000334656.7:c.555G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.178G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3650G>A
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34930
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15097
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr259Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

14-105964144-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964144
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964144
    reference: chr 14
allele count: 46
allele frequency: 2.408881441139506e-3
allele num: 19096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.736C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.565C>G
  hgvsp: ENSP00000333010.7:p.Leu189Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.403C>G
  hgvsp: ENSP00000400014.1:p.Leu135Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.182C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.559C>G
  hgvsp: ENSP00000333959.7:p.Leu187Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.247C>G
  hgvsp: ENSP00000391436.1:p.Leu83Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*207C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.658C>G
  hgvsp: ENSP00000400604.1:p.Leu220Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.682C>G
  hgvsp: ENSP00000346568.6:p.Leu228Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3654C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.988C>G
  hgvsp: ENSP00000376308.4:p.Leu330Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.559C>G
  hgvsp: ENSP00000376312.1:p.Leu187Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.781C>G
  hgvsp: ENSP00000376307.3:p.Leu261Val
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 1.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 34920
  bin: 7.5e0
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14730
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu261Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

14-105964147-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964147
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964147
    reference: chr 14
allele count: 1
allele frequency: 5.068423720223011e-5
allele num: 19730
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*210G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.739G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3657G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.562G>T
  hgvsp: ENSP00000376312.1:p.Gly188Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.250G>T
  hgvsp: ENSP00000391436.1:p.Gly84Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.685G>T
  hgvsp: ENSP00000346568.6:p.Gly229Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.568G>T
  hgvsp: ENSP00000333010.7:p.Gly190Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.661G>T
  hgvsp: ENSP00000400604.1:p.Gly221Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.991G>T
  hgvsp: ENSP00000376308.4:p.Gly331Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.185G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.784G>T
  hgvsp: ENSP00000376307.3:p.Gly262Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.406G>T
  hgvsp: ENSP00000400014.1:p.Gly136Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.562G>T
  hgvsp: ENSP00000333959.7:p.Gly188Cys
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14392
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34924
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly262Cys
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

14-105964150-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964150
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964150
    reference: chr 14
allele count: 1
allele frequency: 4.888541259288228e-5
allele num: 20456
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.253A>G
  hgvsp: ENSP00000391436.1:p.Thr85Ala
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.994A>G
  hgvsp: ENSP00000376308.4:p.Thr332Ala
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.565A>G
  hgvsp: ENSP00000333959.7:p.Thr189Ala
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.571A>G
  hgvsp: ENSP00000333010.7:p.Thr191Ala
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.188A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.409A>G
  hgvsp: ENSP00000400014.1:p.Thr137Ala
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.664A>G
  hgvsp: ENSP00000400604.1:p.Thr222Ala
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.565A>G
  hgvsp: ENSP00000376312.1:p.Thr189Ala
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.787A>G
  hgvsp: ENSP00000376307.3:p.Thr263Ala
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.688A>G
  hgvsp: ENSP00000346568.6:p.Thr230Ala
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*213A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3660A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.742A>G
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14200
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr263Ala
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

14-105964159-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964159
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964159
    reference: chr 14
allele count: 1
allele frequency: 4.539676775013619e-5
allele num: 22028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.197C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1003C>T
  hgvsp: ENSP00000376308.4:p.Pro335Ser
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.418C>T
  hgvsp: ENSP00000400014.1:p.Pro140Ser
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.574C>T
  hgvsp: ENSP00000376312.1:p.Pro192Ser
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.796C>T
  hgvsp: ENSP00000376307.3:p.Pro266Ser
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3669C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.673C>T
  hgvsp: ENSP00000400604.1:p.Pro225Ser
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*222C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.751C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.262C>T
  hgvsp: ENSP00000391436.1:p.Pro88Ser
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.697C>T
  hgvsp: ENSP00000346568.6:p.Pro233Ser
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.574C>T
  hgvsp: ENSP00000333959.7:p.Pro192Ser
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.580C>T
  hgvsp: ENSP00000333010.7:p.Pro194Ser
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14582
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4462
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro266Ser
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ

14-105964160-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964160
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964160
    reference: chr 14
allele count: 2
allele frequency: 9.021199819576004e-5
allele num: 22170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*223C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1004C>T
  hgvsp: ENSP00000376308.4:p.Pro335Leu
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.581C>T
  hgvsp: ENSP00000333010.7:p.Pro194Leu
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.263C>T
  hgvsp: ENSP00000391436.1:p.Pro88Leu
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3670C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.698C>T
  hgvsp: ENSP00000346568.6:p.Pro233Leu
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.419C>T
  hgvsp: ENSP00000400014.1:p.Pro140Leu
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.575C>T
  hgvsp: ENSP00000333959.7:p.Pro192Leu
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.674C>T
  hgvsp: ENSP00000400604.1:p.Pro225Leu
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.575C>T
  hgvsp: ENSP00000376312.1:p.Pro192Leu
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.797C>T
  hgvsp: ENSP00000376307.3:p.Pro266Leu
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.752C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.198C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33463
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14501
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4494
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro266Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

14-105964161-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964161
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964161
    reference: chr 14
allele count: 1
allele frequency: 4.446025253423439e-5
allele num: 22492
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.576G>A
  hgvsp: ENST00000334656.7:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3671G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.582G>A
  hgvsp: ENST00000329886.7:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*224G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.675G>A
  hgvsp: ENST00000432805.1:c.675G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.753G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1005G>A
  hgvsp: ENST00000392523.4:c.1005G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.199G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.420G>A
  hgvsp: ENST00000421892.1:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.798G>A
  hgvsp: ENST00000392522.3:c.798G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.576G>A
  hgvsp: ENST00000392527.1:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.699G>A
  hgvsp: ENST00000354560.6:c.699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.264G>A
  hgvsp: ENST00000450383.1:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 14667
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro266Pro
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

14-105964184-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964184
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964184
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 25566
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.605A>G
  hgvsp: ENSP00000333010.7:p.Gln202Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.443A>G
  hgvsp: ENSP00000400014.1:p.Gln148Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.599A>G
  hgvsp: ENSP00000376312.1:p.Gln200Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.287A>G
  hgvsp: ENSP00000391436.1:p.Gln96Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*247A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.821A>G
  hgvsp: ENSP00000376307.3:p.Gln274Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.599A>G
  hgvsp: ENSP00000333959.7:p.Gln200Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1028A>G
  hgvsp: ENSP00000376308.4:p.Gln343Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3694A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.222A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.698A>G
  hgvsp: ENSP00000400604.1:p.Gln233Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.722A>G
  hgvsp: ENSP00000346568.6:p.Gln241Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.776A>G
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18420
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27744
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln274Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP

14-105964186-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964186
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964186
    reference: chr 14
allele count: 4
allele frequency: 1.569119723834929e-4
allele num: 25492
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*249C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.607C>G
  hgvsp: ENSP00000333010.7:p.Pro203Ala
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.445C>G
  hgvsp: ENSP00000400014.1:p.Pro149Ala
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.778C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1030C>G
  hgvsp: ENSP00000376308.4:p.Pro344Ala
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.601C>G
  hgvsp: ENSP00000333959.7:p.Pro201Ala
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.724C>G
  hgvsp: ENSP00000346568.6:p.Pro242Ala
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.823C>G
  hgvsp: ENSP00000376307.3:p.Pro275Ala
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.289C>G
  hgvsp: ENSP00000391436.1:p.Pro97Ala
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.700C>G
  hgvsp: ENSP00000400604.1:p.Pro234Ala
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.224C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3696C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.601C>G
  hgvsp: ENSP00000376312.1:p.Pro201Ala
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18912
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro275Ala
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-105964187-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964187
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964187
    reference: chr 14
allele count: 18
allele frequency: 7.073247406475951e-4
allele num: 25448
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*250C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.602C>G
  hgvsp: ENSP00000333959.7:p.Pro201Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.290C>G
  hgvsp: ENSP00000391436.1:p.Pro97Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.779C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.824C>G
  hgvsp: ENSP00000376307.3:p.Pro275Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1031C>G
  hgvsp: ENSP00000376308.4:p.Pro344Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.701C>G
  hgvsp: ENSP00000400604.1:p.Pro234Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.608C>G
  hgvsp: ENSP00000333010.7:p.Pro203Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.725C>G
  hgvsp: ENSP00000346568.6:p.Pro242Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.446C>G
  hgvsp: ENSP00000400014.1:p.Pro149Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.602C>G
  hgvsp: ENSP00000376312.1:p.Pro201Arg
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3697C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.225C>G
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26890
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3904
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4927
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Pro275Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

14-105964191-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964191
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964191
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 25270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.229C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.729C>T
  hgvsp: ENST00000354560.6:c.729C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.828C>T
  hgvsp: ENST00000392522.3:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.606C>T
  hgvsp: ENST00000334656.7:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.705C>T
  hgvsp: ENST00000432805.1:c.705C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3701C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.294C>T
  hgvsp: ENST00000450383.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.606C>T
  hgvsp: ENST00000392527.1:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.612C>T
  hgvsp: ENST00000329886.7:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1035C>T
  hgvsp: ENST00000392523.4:c.1035C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.783C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.450C>T
  hgvsp: ENST00000421892.1:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*254C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25666
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20434
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr276Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

14-105964209-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964209
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964209
    reference: chr 14
allele count: 2
allele frequency: 8.555051758063137e-5
allele num: 23378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*272C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.846C>T
  hgvsp: ENST00000392522.3:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3719C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1053C>T
  hgvsp: ENST00000392523.4:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.801C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.468C>T
  hgvsp: ENST00000421892.1:c.468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.747C>T
  hgvsp: ENST00000354560.6:c.747C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.624C>T
  hgvsp: ENST00000392527.1:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.312C>T
  hgvsp: ENST00000450383.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.624C>T
  hgvsp: ENST00000334656.7:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.723C>T
  hgvsp: ENST00000432805.1:c.723C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.630C>T
  hgvsp: ENST00000329886.7:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.247C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20035
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25787
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro282Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum

14-105964210-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964210
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964210
    reference: chr 14
allele count: 3
allele frequency: 1.303667651660003e-4
allele num: 23012
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.631G>A
  hgvsp: ENSP00000333010.7:p.Glu211Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.847G>A
  hgvsp: ENSP00000376307.3:p.Glu283Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.248G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.724G>A
  hgvsp: ENSP00000400604.1:p.Glu242Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.625G>A
  hgvsp: ENSP00000376312.1:p.Glu209Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.748G>A
  hgvsp: ENSP00000346568.6:p.Glu250Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.802G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.313G>A
  hgvsp: ENSP00000391436.1:p.Glu105Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.625G>A
  hgvsp: ENSP00000333959.7:p.Glu209Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400014
  ensembl transcript: ENST00000421892
  gene symbol: C14orf80
  hgvsc: ENST00000421892.1:c.469G>A
  hgvsp: ENSP00000400014.1:p.Glu157Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1054G>A
  hgvsp: ENSP00000376308.4:p.Glu352Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3720G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*273G>A
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19454
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26421
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu283Lys
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

14-105964213-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964213
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964213
    reference: chr 14
allele count: 11
allele frequency: 4.817799579537491e-4
allele num: 22832
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.316C>T
  hgvsp: ENSP00000391436.1:p.Arg106Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.628C>T
  hgvsp: ENSP00000376312.1:p.Arg210Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.634C>T
  hgvsp: ENSP00000333010.7:p.Arg212Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.850C>T
  hgvsp: ENSP00000376307.3:p.Arg284Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.751C>T
  hgvsp: ENSP00000346568.6:p.Arg251Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.727C>T
  hgvsp: ENSP00000400604.1:p.Arg243Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3723C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.628C>T
  hgvsp: ENSP00000333959.7:p.Arg210Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1057C>T
  hgvsp: ENSP00000376308.4:p.Arg353Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.251C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*276C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.805C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18856
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26984
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg284Cys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

14-105964214-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964214
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964214
    reference: chr 14
allele count: 3
allele frequency: 1.352813852813853e-4
allele num: 22176
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*277G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.317G>A
  hgvsp: ENSP00000391436.1:p.Arg106His
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3724G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.728G>A
  hgvsp: ENSP00000400604.1:p.Arg243His
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.851G>A
  hgvsp: ENSP00000376307.3:p.Arg284His
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1058G>A
  hgvsp: ENSP00000376308.4:p.Arg353His
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.635G>A
  hgvsp: ENSP00000333010.7:p.Arg212His
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.806G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.629G>A
  hgvsp: ENSP00000333959.7:p.Arg210His
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.752G>A
  hgvsp: ENSP00000346568.6:p.Arg251His
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.252G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.629G>A
  hgvsp: ENSP00000376312.1:p.Arg210His
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27757
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17952
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg284His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

14-105964215-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964215
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964215
    reference: chr 14
allele count: 1
allele frequency: 4.503693028283192e-5
allele num: 22204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.318C>G
  hgvsp: ENST00000450383.1:c.318C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.630C>G
  hgvsp: ENST00000334656.7:c.630C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.253C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.852C>G
  hgvsp: ENST00000392522.3:c.852C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.636C>G
  hgvsp: ENST00000329886.7:c.636C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*278C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.630C>G
  hgvsp: ENST00000392527.1:c.630C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1059C>G
  hgvsp: ENST00000392523.4:c.1059C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.729C>G
  hgvsp: ENST00000432805.1:c.729C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.807C>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.753C>G
  hgvsp: ENST00000354560.6:c.753C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3725C>G
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27816
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg284Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

14-105964222-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964222
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964222
    reference: chr 14
allele count: 1
allele frequency: 4.593477262287552e-5
allele num: 21770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.325G>A
  hgvsp: ENSP00000391436.1:p.Gly109Ser
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.859G>A
  hgvsp: ENSP00000376307.3:p.Gly287Ser
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.814G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.637G>A
  hgvsp: ENSP00000376312.1:p.Gly213Ser
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3732G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.760G>A
  hgvsp: ENSP00000346568.6:p.Gly254Ser
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.260G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.643G>A
  hgvsp: ENSP00000333010.7:p.Gly215Ser
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.637G>A
  hgvsp: ENSP00000333959.7:p.Gly213Ser
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1066G>A
  hgvsp: ENSP00000376308.4:p.Gly356Ser
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.736G>A
  hgvsp: ENSP00000400604.1:p.Gly246Ser
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*285G>A
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28920
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16909
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly287Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

14-105964224-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964224
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964224
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 21534
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.327C>T
  hgvsp: ENST00000450383.1:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.861C>T
  hgvsp: ENST00000392522.3:c.861C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*287C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.738C>T
  hgvsp: ENST00000432805.1:c.738C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.262C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.762C>T
  hgvsp: ENST00000354560.6:c.762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3734C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1068C>T
  hgvsp: ENST00000392523.4:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.645C>T
  hgvsp: ENST00000329886.7:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.639C>T
  hgvsp: ENST00000392527.1:c.639C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.639C>T
  hgvsp: ENST00000334656.7:c.639C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.816C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 16398
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29303
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly287Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

14-105964225-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964225
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964225
    reference: chr 14
allele count: 8
allele frequency: 3.709886848451122e-4
allele num: 21564
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.817G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.640G>A
  hgvsp: ENSP00000376312.1:p.Glu214Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.328G>A
  hgvsp: ENSP00000391436.1:p.Glu110Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.739G>A
  hgvsp: ENSP00000400604.1:p.Glu247Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*288G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1069G>A
  hgvsp: ENSP00000376308.4:p.Glu357Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.646G>A
  hgvsp: ENSP00000333010.7:p.Glu216Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.640G>A
  hgvsp: ENSP00000333959.7:p.Glu214Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.763G>A
  hgvsp: ENSP00000346568.6:p.Glu255Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.862G>A
  hgvsp: ENSP00000376307.3:p.Glu288Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.263G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3735G>A
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29383
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5059
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu288Lys
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

14-105964243-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964243
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964243
    reference: chr 14
allele count: 4
allele frequency: 1.952171791117618e-4
allele num: 20490
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.664C>T
  hgvsp: ENSP00000333010.7:p.Arg222Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1087C>T
  hgvsp: ENSP00000376308.4:p.Arg363Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3753C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.880C>T
  hgvsp: ENSP00000376307.3:p.Arg294Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.346C>T
  hgvsp: ENSP00000391436.1:p.Arg116Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.781C>T
  hgvsp: ENSP00000346568.6:p.Arg261Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.658C>T
  hgvsp: ENSP00000333959.7:p.Arg220Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.281C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.757C>T
  hgvsp: ENSP00000400604.1:p.Arg253Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*306C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.835C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.658C>T
  hgvsp: ENSP00000376312.1:p.Arg220Trp
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11582
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg294Trp
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-105964244-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964244
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964244
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 20208
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.665G>A
  hgvsp: ENSP00000333010.7:p.Arg222Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1088G>A
  hgvsp: ENSP00000376308.4:p.Arg363Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.659G>A
  hgvsp: ENSP00000333959.7:p.Arg220Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.782G>A
  hgvsp: ENSP00000346568.6:p.Arg261Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.758G>A
  hgvsp: ENSP00000400604.1:p.Arg253Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.347G>A
  hgvsp: ENSP00000391436.1:p.Arg116Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.881G>A
  hgvsp: ENSP00000376307.3:p.Arg294Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*307G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.282G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.659G>A
  hgvsp: ENSP00000376312.1:p.Arg220Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3754G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.836G>A
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 32622
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10912
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg294Gln
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

14-105964245-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964245
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964245
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 20276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.759G>C
  hgvsp: ENST00000432805.1:c.759G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.783G>C
  hgvsp: ENST00000354560.6:c.783G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.660G>C
  hgvsp: ENST00000392527.1:c.660G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.882G>C
  hgvsp: ENST00000392522.3:c.882G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1089G>C
  hgvsp: ENST00000392523.4:c.1089G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.348G>C
  hgvsp: ENST00000450383.1:c.348G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.666G>C
  hgvsp: ENST00000329886.7:c.666G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3755G>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.660G>C
  hgvsp: ENST00000334656.7:c.660G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.283G>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*308G>C
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.837G>C
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10890
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32699
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg294Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

14-105964256-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964256
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964256
    reference: chr 14
allele count: 35
allele frequency: 1.769285208775655e-3
allele num: 19782
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.294C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.794C>T
  hgvsp: ENSP00000346568.6:p.Ala265Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.671C>T
  hgvsp: ENSP00000376312.1:p.Ala224Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*319C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1100C>T
  hgvsp: ENSP00000376308.4:p.Ala367Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.893C>T
  hgvsp: ENSP00000376307.3:p.Ala298Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.770C>T
  hgvsp: ENSP00000400604.1:p.Ala257Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3766C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.677C>T
  hgvsp: ENSP00000333010.7:p.Ala226Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.671C>T
  hgvsp: ENSP00000333959.7:p.Ala224Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.359C>T
  hgvsp: ENSP00000391436.1:p.Ala120Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.848C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33164
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9332
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala298Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS

14-105964257-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964257
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964257
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 19724
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1101A>G
  hgvsp: ENST00000392523.4:c.1101A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.894A>G
  hgvsp: ENST00000392522.3:c.894A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.360A>G
  hgvsp: ENST00000450383.1:c.360A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3767A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.672A>G
  hgvsp: ENST00000334656.7:c.672A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.771A>G
  hgvsp: ENST00000432805.1:c.771A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.295A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.795A>G
  hgvsp: ENST00000354560.6:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.678A>G
  hgvsp: ENST00000329886.7:c.678A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.672A>G
  hgvsp: ENST00000392527.1:c.672A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*320A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.849A>G
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9128
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala298Ala
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

14-105964264-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964264
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964264
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 19096
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.302G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*327G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.901G>A
  hgvsp: ENSP00000376307.3:p.Glu301Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.856G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3774G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.778G>A
  hgvsp: ENSP00000400604.1:p.Glu260Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.802G>A
  hgvsp: ENSP00000346568.6:p.Glu268Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1108G>A
  hgvsp: ENSP00000376308.4:p.Glu370Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.367G>A
  hgvsp: ENSP00000391436.1:p.Glu123Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.679G>A
  hgvsp: ENSP00000376312.1:p.Glu227Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.685G>A
  hgvsp: ENSP00000333010.7:p.Glu229Lys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.679G>A
  hgvsp: ENSP00000333959.7:p.Glu227Lys
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33384
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu301Lys
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

14-105964267-G-GAGCTGCGGGA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964267
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964277
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 18686
alternate allele: GAGCTGCGGGA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsp: ENSP00000376308.4:p.Glu377GlyfsTer198
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsp: ENSP00000376312.1:p.Glu234GlyfsTer198
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsp: ENSP00000391436.1:p.Glu130GlyfsTer?
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsp: ENSP00000333010.7:p.Glu236GlyfsTer198
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsp: ENSP00000346568.6:p.Glu275GlyfsTer198
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsp: ENSP00000400604.1:p.Glu267GlyfsTer?
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsp: ENSP00000376307.3:p.Glu308GlyfsTer?
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsp: ENSP00000333959.7:p.Glu234GlyfsTer198
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6974
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu308GlyfsTer?
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

14-105964270-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964270
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964270
    reference: chr 14
allele count: 2
allele frequency: 1.148897058823529e-4
allele num: 17408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1114C>T
  hgvsp: ENST00000392523.4:c.1114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.907C>T
  hgvsp: ENST00000392522.3:c.907C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.685C>T
  hgvsp: ENST00000392527.1:c.685C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.685C>T
  hgvsp: ENST00000334656.7:c.685C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.808C>T
  hgvsp: ENST00000354560.6:c.808C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.784C>T
  hgvsp: ENST00000432805.1:c.784C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.373C>T
  hgvsp: ENST00000450383.1:c.373C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.691C>T
  hgvsp: ENST00000329886.7:c.691C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.308C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*333C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3780C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.862C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32483
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5948
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu303Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

14-105964273-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964273
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964273
    reference: chr 14
allele count: 1
allele frequency: 5.730002292000917e-5
allele num: 17452
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.910C>T
  hgvsp: ENSP00000376307.3:p.Arg304Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.811C>T
  hgvsp: ENSP00000346568.6:p.Arg271Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3783C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.787C>T
  hgvsp: ENSP00000400604.1:p.Arg263Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.694C>T
  hgvsp: ENSP00000333010.7:p.Arg232Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.376C>T
  hgvsp: ENSP00000391436.1:p.Arg126Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1117C>T
  hgvsp: ENSP00000376308.4:p.Arg373Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.865C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.688C>T
  hgvsp: ENSP00000376312.1:p.Arg230Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*336C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.688C>T
  hgvsp: ENSP00000333959.7:p.Arg230Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.311C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5887
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32704
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg304Trp
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum

14-105964274-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964274
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964274
    reference: chr 14
allele count: 2
allele frequency: 1.143249113981937e-4
allele num: 17494
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.377G>A
  hgvsp: ENSP00000391436.1:p.Arg126Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.695G>A
  hgvsp: ENSP00000333010.7:p.Arg232Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1118G>A
  hgvsp: ENSP00000376308.4:p.Arg373Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.812G>A
  hgvsp: ENSP00000346568.6:p.Arg271Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*337G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.689G>A
  hgvsp: ENSP00000376312.1:p.Arg230Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.788G>A
  hgvsp: ENSP00000400604.1:p.Arg263Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.866G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.911G>A
  hgvsp: ENSP00000376307.3:p.Arg304Gln
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3784G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.312G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.689G>A
  hgvsp: ENSP00000333959.7:p.Arg230Gln
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5865
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32795
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg304Gln
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ

14-105964284-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964284
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964284
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 16158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.798G>A
  hgvsp: ENST00000432805.1:c.798G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.921G>A
  hgvsp: ENST00000392522.3:c.921G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.699G>A
  hgvsp: ENST00000392527.1:c.699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1128G>A
  hgvsp: ENST00000392523.4:c.1128G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.387G>A
  hgvsp: ENST00000450383.1:c.387G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.322G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3794G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.822G>A
  hgvsp: ENST00000354560.6:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*347G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.705G>A
  hgvsp: ENST00000329886.7:c.705G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.699G>A
  hgvsp: ENST00000334656.7:c.699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.876G>A
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31816
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala307Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

14-105964288-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964288
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964288
    reference: chr 14
allele count: 1
allele frequency: 6.855889208830385e-5
allele num: 14586
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.391C>T
  hgvsp: ENSP00000391436.1:p.Arg131Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.703C>T
  hgvsp: ENSP00000333959.7:p.Arg235Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*351C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.826C>T
  hgvsp: ENSP00000346568.6:p.Arg276Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.925C>T
  hgvsp: ENSP00000376307.3:p.Arg309Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.703C>T
  hgvsp: ENSP00000376312.1:p.Arg235Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.709C>T
  hgvsp: ENSP00000333010.7:p.Arg237Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.802C>T
  hgvsp: ENSP00000400604.1:p.Arg268Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1132C>T
  hgvsp: ENSP00000376308.4:p.Arg378Cys
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.880C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3798C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.326C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29301
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg309Cys
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

14-105964289-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964289
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964289
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 14640
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1133G>A
  hgvsp: ENSP00000376308.4:p.Arg378His
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.710G>A
  hgvsp: ENSP00000333010.7:p.Arg237His
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.803G>A
  hgvsp: ENSP00000400604.1:p.Arg268His
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.392G>A
  hgvsp: ENSP00000391436.1:p.Arg131His
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.926G>A
  hgvsp: ENSP00000376307.3:p.Arg309His
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.827G>A
  hgvsp: ENSP00000346568.6:p.Arg276His
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3799G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.704G>A
  hgvsp: ENSP00000333959.7:p.Arg235His
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.704G>A
  hgvsp: ENSP00000376312.1:p.Arg235His
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.327G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*352G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.881G>A
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 29407
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3905
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg309His
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-105964294-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964294
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964294
    reference: chr 14
allele count: 4
allele frequency: 2.834467120181406e-4
allele num: 14112
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.808C>T
  hgvsp: ENSP00000400604.1:p.Arg270Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.715C>T
  hgvsp: ENSP00000333010.7:p.Arg239Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.832C>T
  hgvsp: ENSP00000346568.6:p.Arg278Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.709C>T
  hgvsp: ENSP00000376312.1:p.Arg237Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1138C>T
  hgvsp: ENSP00000376308.4:p.Arg380Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3804C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*357C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.886C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.397C>T
  hgvsp: ENSP00000391436.1:p.Arg133Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.931C>T
  hgvsp: ENSP00000376307.3:p.Arg311Trp
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.332C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.709C>T
  hgvsp: ENSP00000333959.7:p.Arg237Trp
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28539
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg311Trp
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

14-105964298-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964298
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964298
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 13542
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3808C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*361C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.336C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.812C>T
  hgvsp: ENSP00000400604.1:p.Ala271Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.713C>T
  hgvsp: ENSP00000333959.7:p.Ala238Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.719C>T
  hgvsp: ENSP00000333010.7:p.Ala240Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.713C>T
  hgvsp: ENSP00000376312.1:p.Ala238Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.935C>T
  hgvsp: ENSP00000376307.3:p.Ala312Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.401C>T
  hgvsp: ENSP00000391436.1:p.Ala134Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1142C>T
  hgvsp: ENSP00000376308.4:p.Ala381Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.836C>T
  hgvsp: ENSP00000346568.6:p.Ala279Val
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.890C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27549
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala312Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

14-105964299-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964299
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964299
    reference: chr 14
allele count: 1
allele frequency: 7.48502994011976e-5
allele num: 13360
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1143G>A
  hgvsp: ENST00000392523.4:c.1143G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.936G>A
  hgvsp: ENST00000392522.3:c.936G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.891G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.402G>A
  hgvsp: ENST00000450383.1:c.402G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.813G>A
  hgvsp: ENST00000432805.1:c.813G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.720G>A
  hgvsp: ENST00000329886.7:c.720G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3809G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.337G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.714G>A
  hgvsp: ENST00000392527.1:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*362G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.837G>A
  hgvsp: ENST00000354560.6:c.837G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.714G>A
  hgvsp: ENST00000334656.7:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26789
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala312Ala
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

14-105964322-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964322
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964322
    reference: chr 14
allele count: 1
allele frequency: 8.733624454148471e-5
allele num: 11450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.352+8C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3824+8C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.951+8C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.906+8C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.729+8C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.852+8C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.828+8C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.729+8C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.735+8C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1158+8C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.417+8C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*377+8C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.951+8C>T
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

14-105964329-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964329
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964329
    reference: chr 14
allele count: 6
allele frequency: 5.610622779128483e-4
allele num: 10694
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.729+15C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.828+15C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3824+15C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.352+15C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.417+15C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.729+15C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.852+15C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.951+15C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.906+15C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.735+15C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*377+15C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1158+15C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3056
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP

14-105964330-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964330
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964330
    reference: chr 14
allele count: 1
allele frequency: 9.489466691971911e-5
allele num: 10538
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3824+16G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.352+16G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.951+16G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.417+16G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.735+16G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.852+16G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.906+16G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.729+16G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.828+16G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*377+16G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1158+16G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.729+16G>A
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ

14-105964340-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964340
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964340
    reference: chr 14
allele count: 1
allele frequency: 1.05909764880322e-4
allele num: 9442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.735+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*377+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.729+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.729+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1158+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.951+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.828+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.352+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.906+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.852+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.417+26C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3824+26C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3635
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

14-105964342-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964342
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964342
    reference: chr 14
allele count: 267
allele frequency: 2.792302865509308e-2
allele num: 9562
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.906+28A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.735+28A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.729+28A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.852+28A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.352+28A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.729+28A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.951+28A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.828+28A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.417+28A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3824+28A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*377+28A>G
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1158+28A>G
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3676
  bin: 7.5e0
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 2.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 1.25e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 1.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 21180
  bin: 2.5e0
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 20
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

14-105964358-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964358
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964358
    reference: chr 14
allele count: 36
allele frequency: 4.74308300395257e-3
allele num: 7590
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.352+44C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.906+44C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.828+44C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*377+44C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.735+44C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.951+44C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3824+44C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.729+44C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.852+44C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.729+44C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.417+44C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1158+44C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 1.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 7.5e0
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 20776
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

14-105964358-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964358
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964357
    reference: chr 14
allele count: 1
allele frequency: 1.317523056653491e-4
allele num: 7590
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.852+49delG
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3824+49delG
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.729+49delG
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1158+49delG
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.906+49delG
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.729+49delG
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.735+49delG
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.352+49delG
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.951+49delG
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.417+49delG
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.828+49delG
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*377+49delG
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20776
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: CG
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

14-105964359-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964359
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964359
    reference: chr 14
allele count: 1
allele frequency: 1.318565400843882e-4
allele num: 7584
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.852+45G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.729+45G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.951+45G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1158+45G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.352+45G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*377+45G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.729+45G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.828+45G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3824+45G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.906+45G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.735+45G>A
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.417+45G>A
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20900
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

14-105964363-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964363
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964363
    reference: chr 14
allele count: 6
allele frequency: 8.156606851549756e-4
allele num: 7356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.729+49G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*377+49G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.352+49G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.852+49G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.417+49G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3824+49G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.729+49G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1158+49G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.951+49G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.906+49G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.828+49G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.735+49G>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20948
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-105964915-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964915
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964915
    reference: chr 14
allele count: 1
allele frequency: 1.833516685001834e-4
allele num: 5454
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*378-39C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376308
  ensembl transcript: ENST00000392523
  gene symbol: C14orf80
  hgvsc: ENST00000392523.4:c.1159-39C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000546492
  gene symbol: C14orf80
  hgvsc: ENST00000546492.1:n.353-39C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333010
  ensembl transcript: ENST00000329886
  gene symbol: C14orf80
  hgvsc: ENST00000329886.7:c.736-39C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.418-39C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3825-39C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.730-39C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.829-39C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.730-39C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376307
  ensembl transcript: ENST00000392522
  gene symbol: C14orf80
  hgvsc: ENST00000392522.3:c.952-39C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.853-39C>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.907-39C>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38991
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum

14-105964921-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 105964921
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 105964921
    reference: chr 14
allele count: 3
allele frequency: 5.343783398646241e-4
allele num: 5614
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000376312
  ensembl transcript: ENST00000392527
  gene symbol: C14orf80
  hgvsc: ENST00000392527.1:c.730-33G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551054
  gene symbol: C14orf80
  hgvsc: ENST00000551054.1:n.907-33G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000400604
  ensembl transcript: ENST00000432805
  gene symbol: C14orf80
  hgvsc: ENST00000432805.1:c.829-33G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000346568
  ensembl transcript: ENST00000354560
  gene symbol: C14orf80
  hgvsc: ENST00000354560.6:c.853-33G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000450003
  ensembl transcript: ENST00000548920
  gene symbol: C14orf80
  hgvsc: ENST00000548920.2:c.*378-33G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000333959
  ensembl transcript: ENST00000334656
  gene symbol: C14orf80
  hgvsc: ENST00000334656.7:c.730-33G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl protein: ENSP00000391436
  ensembl transcript: ENST00000450383
  gene symbol: C14orf80
  hgvsc: ENST00000450383.1:c.418-33G>T
  variant of: http://identifiers.org/hgnc/20127
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185347
  ensembl transcript: ENST00000551538
  gene symbol: C14orf80
  hgvsc: ENST00000551538.1:n.3825-33G>T
  variant of: http://identifiers.org/hgnc/20127
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 909
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1112
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1283
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1241
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 334
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 732
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 686
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4890
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1846
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 871
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32999
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 674
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5409
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1849
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8952
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.561253561253561e-4
allele num: 2808
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7926
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.369668246445498e-3
allele num: 422
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.879999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.099999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.191e1

DP
type: SiteQuality
SIO_000300: 5.82189e5

FS
type: SiteQuality
SIO_000300: 9.0e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e0

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

GenotypeDepth
all individuals: 686
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1282
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 725
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 909
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 98
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1112
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1241
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1704
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5170
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 791
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 33146
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 580
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1843
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4890
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 341
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8946
num of homozygotes: 0

South Asian
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allele frequency: 1.261988894497728e-4
allele num: 7924
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
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SIO_000300: 4.83e-1

FS
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SIO_000300: 2.359e0

QD
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VQSLOD
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ReadPosRankSum
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SIO_000300: -3.58e-1

ClippingRankSum
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SIO_000300: -2.92e-1

InbreedingCoeff
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SIO_000300: -7.140000000000001e-2

DP
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SIO_000300: 5.79546e5

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 8718
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7892
num of homozygotes: 0

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

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

Other
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num of homozygotes: 0

MQRankSum
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SIO_000300: 3.58e-1

FS
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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SIO_000300: 6.0e1

DP
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SIO_000300: 5.46951e5

BaseQRankSum
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SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

GenotypeDepth
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variant carriers: 9

GenotypeDepth
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GenotypeDepth
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variant carriers: 13

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 1

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 28
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

European (Non-Finnish)
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allele count: 102
allele frequency: 1.172953081876725e-2
allele num: 8696
num of homozygotes: 1

VQSLOD
type: SiteQuality
SIO_000300: 4.22e0

InbreedingCoeff
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SIO_000300: -7.56e-2

MQRankSum
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DP
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QD
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BaseQRankSum
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SIO_000300: 3.76e0

MQ
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SIO_000300: 5.987e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -1.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.22e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 675
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GenotypeQuality
all individuals: 560
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2744
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 638
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.149954001839926e-4
allele num: 8696
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 9.949999999999999e0

FS
type: SiteQuality
SIO_000300: 1.625e0

ReadPosRankSum
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SIO_000300: -4.42e-1

VQSLOD
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DP
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SIO_000300: 5.38184e5

BaseQRankSum
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SIO_000300: -2.193e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.542e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-3

MQ
type: SiteQuality
SIO_000300: 5.957e1

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 8696
num of homozygotes: 0

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

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

European (Finnish)
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allele frequency: 0.0e0
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Other
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allele num: 194
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 2.533569799847986e-4
allele num: 7894
num of homozygotes: 0

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

African
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Other
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South Asian
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European (Finnish)
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European (Non-Finnish)
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East Asian
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MQ
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MQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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QD
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BaseQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 1.267748478701826e-4
allele num: 7888
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 402
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2742
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

MQ
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SIO_000300: 5.939e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.01e-1

InbreedingCoeff
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SIO_000300: 6.05e-2

FS
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SIO_000300: 2.547e0

VQSLOD
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SIO_000300: 6.0e-1

QD
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SIO_000300: 1.419e1

DP
type: SiteQuality
SIO_000300: 5.23108e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

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

South Asian
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allele frequency: 1.267748478701826e-4
allele num: 7888
num of homozygotes: 0

African
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allele frequency: 3.652300949598247e-4
allele num: 2738
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.322880371660859e-4
allele num: 8610
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 1.54e0

FS
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SIO_000300: 5.91e-1

InbreedingCoeff
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QD
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ClippingRankSum
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SIO_000300: 4.06e-1

DP
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ReadPosRankSum
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MQRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

African
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allele num: 2720
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

DP
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BaseQRankSum
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SIO_000300: -9.2e-2

ClippingRankSum
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MQ
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VQSLOD
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QD
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SIO_000300: 1.254e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.24e-2

ReadPosRankSum
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SIO_000300: -2.14e-1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2708
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele num: 7870
num of homozygotes: 0

East Asian
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -8.690000000000001e-2

FS
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MQRankSum
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DP
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VQSLOD
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MQ
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SIO_000300: 5.952e1

QD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
allele num: 1182
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 462
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 2.86368843069874e-4
allele num: 6984
num of homozygotes: 0

European (Finnish)
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East Asian
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African
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Other
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MQRankSum
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SIO_000300: 2.48e-1

FS
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BaseQRankSum
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InbreedingCoeff
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QD
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DP
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MQ
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

South Asian
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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Other
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ReadPosRankSum
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MQ
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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FS
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DP
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VQSLOD
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QD
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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African
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European (Finnish)
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South Asian
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European (Non-Finnish)
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Other
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ClippingRankSum
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FS
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MQ
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QD
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VQSLOD
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MQRankSum
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DP
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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African
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European (Finnish)
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European (Non-Finnish)
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QD
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DP
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VQSLOD
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FS
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ReadPosRankSum
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BaseQRankSum
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MQ
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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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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Other
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InbreedingCoeff
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ClippingRankSum
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FS
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ReadPosRankSum
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QD
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MQRankSum
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DP
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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African
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East Asian
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South Asian
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European (Finnish)
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Other
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FS
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QD
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VQSLOD
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DP
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MQ
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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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: 1.255020080321285e-4
allele num: 7968
num of homozygotes: 0

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

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

Latino
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allele count: 3
allele frequency: 4.087193460490463e-3
allele num: 734
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 40
allele frequency: 4.032258064516129e-3
allele num: 9920
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.840909090909091e-3
allele num: 352
num of homozygotes: 0

African
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allele count: 2
allele frequency: 6.788866259334691e-4
allele num: 2946
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e-1

FS
type: SiteQuality
SIO_000300: 1.102e0

QD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -2.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 3.05e0

DP
type: SiteQuality
SIO_000300: 4.98735e5

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.4e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2984
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 9.84251968503937e-5
allele num: 10160
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 358
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3672
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 150
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.94e-2

QD
type: SiteQuality
SIO_000300: 3.54e0

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

BaseQRankSum
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SIO_000300: -6.889999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.783e0

FS
type: SiteQuality
SIO_000300: 1.885e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 102
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GenotypeQuality
all individuals: 1190
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.315649867374005e-4
allele num: 3016
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4020
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10418
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.06e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.06e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.94e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.46e-1

DP
type: SiteQuality
SIO_000300: 5.10889e5

GenotypeDepth
all individuals: 131
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 41
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4872
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3082
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 5.903187721369539e-4
allele num: 1694
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10976
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.97e-2

DP
type: SiteQuality
SIO_000300: 5.18555e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.065e0

QD
type: SiteQuality
SIO_000300: 1.96e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 378
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3084
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1690
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4952
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.81257930034439e-4
allele num: 11034
num of homozygotes: 0

InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

FS
type: SiteQuality
SIO_000300: 1.0146e1

BaseQRankSum
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SIO_000300: 4.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.662e0

DP
type: SiteQuality
SIO_000300: 5.21777e5

QD
type: SiteQuality
SIO_000300: 2.846e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 3116
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 8.999280057595392e-5
allele num: 11112
num of homozygotes: 0

South Asian
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VQSLOD
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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DP
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QD
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InbreedingCoeff
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SIO_000300: -3.04e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 11782
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

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

South Asian
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allele count: 0
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num of homozygotes: 0

InbreedingCoeff
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ClippingRankSum
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MQRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: 0.0e0

FS
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MQ
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SIO_000300: 6.0e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7536
num of homozygotes: 0

African
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allele frequency: 1.266624445851805e-3
allele num: 3158
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 11714
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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VQSLOD
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ClippingRankSum
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MQRankSum
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DP
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QD
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InbreedingCoeff
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MQ
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 11680
num of homozygotes: 0

Latino
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allele frequency: 1.149425287356322e-3
allele num: 870
num of homozygotes: 0

African
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allele count: 17
allele frequency: 5.441741357234315e-3
allele num: 3124
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East Asian
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num of homozygotes: 0

Other
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num of homozygotes: 0

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

South Asian
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VQSLOD
type: SiteQuality
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DP
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FS
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BaseQRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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SIO_000300: -3.93e-2

ClippingRankSum
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SIO_000300: 3.61e-1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 360
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.0843e1

InbreedingCoeff
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DP
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QD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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MQ
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BaseQRankSum
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SIO_000300: -1.652e0

GenotypeDepth
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GenotypeDepth
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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: 1.953506544246923e-4
allele num: 10238
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

South Asian
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African
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Other
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European (Non-Finnish)
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African
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South Asian
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allele num: 7846
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European (Finnish)
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Latino
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BaseQRankSum
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DP
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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ReadPosRankSum
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MQ
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 1238
num of homozygotes: 0

European (Finnish)
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Other
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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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BaseQRankSum
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DP
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VQSLOD
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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QD
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FS
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 3.25e1
variant carriers: 2

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1154
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7828
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 1.090116279069767e-3
allele num: 2752
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.67361e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.69e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.767e-1

BaseQRankSum
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SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 4.383e0

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-1

QD
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SIO_000300: 1.241e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 129
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.050420168067227e-4
allele num: 9520
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2742
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7828
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1160
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.44e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.37e-1

QD
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SIO_000300: 1.134e1

ReadPosRankSum
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SIO_000300: 4.31e-1

FS
type: SiteQuality
SIO_000300: 3.474e0

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-1

BaseQRankSum
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SIO_000300: -9.28e-1

DP
type: SiteQuality
SIO_000300: 4.67213e5

MQ
type: SiteQuality
SIO_000300: 5.943e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
all individuals: 174
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 3.65764447695684e-4
allele num: 2734
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7836
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1030
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9276
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.169e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.75e-2

FS
type: SiteQuality
SIO_000300: 1.623e0

DP
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SIO_000300: 4.60819e5

BaseQRankSum
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SIO_000300: -2.801e0

VQSLOD
type: SiteQuality
SIO_000300: -1.045e0

QD
type: SiteQuality
SIO_000300: 1.121e1

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
all individuals: 1510
bin: 1.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 990
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9124
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2708
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.946e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.57525e5

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 5.219e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 3.48e0

GenotypeDepth
all individuals: 28
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
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variant carriers: 0

GenotypeDepth
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 199
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 308
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GenotypeQuality
all individuals: 786
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2708
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 7.660878447395301e-4
allele num: 7832
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.094091903719913e-4
allele num: 9140
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.01010101010101e-3
allele num: 990
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.27e-1

QD
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SIO_000300: 9.140000000000001e0

InbreedingCoeff
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SIO_000300: -5.88e-2

MQRankSum
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DP
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SIO_000300: 4.57947e5

FS
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SIO_000300: 1.266e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.41e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.34e-1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 3.512058066026691e-4
allele num: 8542
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 1.289324394017535e-4
allele num: 7756
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MQRankSum
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VQSLOD
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BaseQRankSum
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MQ
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DP
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FS
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

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

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 160
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8416
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ClippingRankSum
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SIO_000300: 9.22e-1

InbreedingCoeff
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SIO_000300: -6.710000000000001e-2

DP
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SIO_000300: 4.12891e5

MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 9.22e-1

QD
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SIO_000300: 1.266e1

VQSLOD
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SIO_000300: -2.286e0

ReadPosRankSum
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SIO_000300: -9.22e-1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 33

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 3

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2554
num of homozygotes: 0

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

South Asian
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allele count: 34
allele frequency: 4.449097095001309e-3
allele num: 7642
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 8170
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 2.5e-3
allele num: 400
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.96594e5

MQRankSum
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SIO_000300: 1.58e-1

BaseQRankSum
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ClippingRankSum
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SIO_000300: -9.2e-2

ReadPosRankSum
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QD
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VQSLOD
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SIO_000300: -4.767e-1

InbreedingCoeff
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SIO_000300: -6.93e-2

MQ
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SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.152e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 402
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7616
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
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SIO_000300: -1.231e0

MQRankSum
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SIO_000300: 1.23e0

MQ
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ReadPosRankSum
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SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -7.000000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.93e-2

DP
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SIO_000300: 3.93553e5

QD
type: SiteQuality
SIO_000300: 6.16e0

GenotypeDepth
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bin: 3.25e1
variant carriers: 0

GenotypeDepth
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bin: 7.75e1
variant carriers: 0

GenotypeDepth
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7484
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 698
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2456
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7836
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -1.754e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -7.28e-2

DP
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ClippingRankSum
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SIO_000300: -9.370000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.432e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

QD
type: SiteQuality
SIO_000300: 5.15e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7358
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 7660
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.61078e5

MQRankSum
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FS
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BaseQRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: -7.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

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

South Asian
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African
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allele num: 2248
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DP
type: SiteQuality
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VQSLOD
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FS
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MQ
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

Latino
type: Population
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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East Asian
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South Asian
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allele num: 6944
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BaseQRankSum
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SIO_000300: 7.27e-1

DP
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InbreedingCoeff
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VQSLOD
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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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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 2.873563218390805e-4
allele num: 6960
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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num of homozygotes: 0

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

Latino
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Other
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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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African
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European (Finnish)
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BaseQRankSum
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QD
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FS
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DP
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InbreedingCoeff
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VQSLOD
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MQRankSum
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MQ
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 2.551020408163265e-3
allele num: 392
num of homozygotes: 0

Latino
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African
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Other
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European (Non-Finnish)
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European (Finnish)
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South Asian
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BaseQRankSum
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MQRankSum
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MQ
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DP
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FS
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QD
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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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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East Asian
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European (Finnish)
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Other
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Latino
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South Asian
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African
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QD
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ReadPosRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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VQSLOD
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FS
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DP
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ClippingRankSum
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BaseQRankSum
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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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Latino
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East Asian
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European (Non-Finnish)
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European (Finnish)
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African
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South Asian
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QD
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FS
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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DP
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MQ
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InbreedingCoeff
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ClippingRankSum
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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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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4680
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1788
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.976190476190476e-3
allele num: 336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4768
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4182
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.00498e5

MQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

QD
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SIO_000300: 1.26e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.679e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.96e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.49e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

GenotypeDepth
all individuals: 35
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 8.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 35
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4514
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 324
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1722
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 1.592356687898089e-3
allele num: 3768
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 108
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.99e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-1

FS
type: SiteQuality
SIO_000300: 2.209e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.16e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

DP
type: SiteQuality
SIO_000300: 1.90441e5

GenotypeDepth
all individuals: 77
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 254
bin: 3.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.708559046587215e-4
allele num: 3692
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 104
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1708
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4466
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.151e1

MQRankSum
type: SiteQuality
SIO_000300: -1.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.555e0

FS
type: SiteQuality
SIO_000300: 1.243e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.03e-2

VQSLOD
type: SiteQuality
SIO_000300: -8.847e-1

DP
type: SiteQuality
SIO_000300: 1.89524e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 35
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 6.476683937823834e-4
allele num: 1544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4102
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 98
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.29e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.643e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.617e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.89e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.085e0

DP
type: SiteQuality
SIO_000300: 1.76999e5

QD
type: SiteQuality
SIO_000300: 1.399e1

GenotypeDepth
all individuals: 30
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 555
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 38
bin: 9.25e1
variant carriers: 8

GenotypeQuality
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variant carriers: 7

GenotypeQuality
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bin: 6.25e1
variant carriers: 7

GenotypeQuality
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variant carriers: 4

GenotypeQuality
all individuals: 16976
bin: 7.5e0
variant carriers: 27

GenotypeQuality
all individuals: 47
bin: 4.75e1
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GenotypeQuality
all individuals: 611
bin: 2.75e1
variant carriers: 5

GenotypeQuality
all individuals: 4435
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 218
bin: 3.75e1
variant carriers: 6

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 30
bin: 8.75e1
variant carriers: 8

GenotypeQuality
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GenotypeQuality
all individuals: 852
bin: 9.75e1
variant carriers: 235

GenotypeQuality
all individuals: 601
bin: 3.25e1
variant carriers: 5

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 5

GenotypeQuality
all individuals: 4244
bin: 2.25e1
variant carriers: 8

GenotypeQuality
all individuals: 71
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 29
bin: 7.25e1
variant carriers: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

African
type: Population
allele count: 262
allele frequency: 1.633416458852868e-1
allele num: 1604
num of homozygotes: 20

Latino
type: Population
allele count: 2
allele frequency: 8.928571428571428e-3
allele num: 224
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 7.274490785645005e-4
allele num: 4124
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 1.77682e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.88e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.554e1

GenotypeDepth
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 3

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 575
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 66
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variant carriers: 3

GenotypeQuality
all individuals: 29
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 685
bin: 9.75e1
variant carriers: 30

GenotypeQuality
all individuals: 246
bin: 6.25e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 8.305647840531562e-4
allele num: 1204
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.933701657458564e-3
allele num: 3620
num of homozygotes: 0

South Asian
type: Population
allele count: 28
allele frequency: 1.285583103764922e-2
allele num: 2178
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 300
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

QD
type: SiteQuality
SIO_000300: 1.345e1

VQSLOD
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SIO_000300: 1.05e0

BaseQRankSum
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SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.669e0

DP
type: SiteQuality
SIO_000300: 1.63727e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.950000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 564
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variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 300
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2178
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.76243093922652e-4
allele num: 3620
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-2

MQRankSum
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BaseQRankSum
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VQSLOD
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FS
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.345e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.950000000000001e-2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 256
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variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2168
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.75330396475771e-4
allele num: 3632
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.715e1

DP
type: SiteQuality
SIO_000300: 1.63871e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.95e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.37e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.733e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeDepth
all individuals: 58
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1320
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13355
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 251
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2783
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1120
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7944
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 660
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 9.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 8.333333333333334e-4
allele num: 1200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 8.337965536409116e-4
allele num: 3598
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.012145748987854e-3
allele num: 1976
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

DP
type: SiteQuality
SIO_000300: 1.64469e5

QD
type: SiteQuality
SIO_000300: 1.218e1

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.78e-1

GenotypeDepth
all individuals: 8
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1663
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6897
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30410
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 250
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 321
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3485
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3064
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 802
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1088
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2956
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.890000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.036e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.947e0

MQ
type: SiteQuality
SIO_000300: 5.829e1

DP
type: SiteQuality
SIO_000300: 1.99821e5

QD
type: SiteQuality
SIO_000300: 3.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.41e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.41e-1