6-43039593-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039593
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039593
    reference: chr 6
allele count: 8
allele frequency: 7.953076846605031e-5
allele num: 100590
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1312C>T
  hgvsp: ENSP00000418031.1:p.Arg438Trp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*894C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1081C>T
  hgvsp: ENSP00000395806.2:p.Arg361Trp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1366C>T
  hgvsp: ENSP00000259708.3:p.Arg456Trp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1312C>T
  hgvsp: ENSP00000340221.5:p.Arg438Trp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.433+236C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1312C>T
  hgvsp: ENSP00000377622.1:p.Arg438Trp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1312C>T
  hgvsp: ENSP00000377620.2:p.Arg438Trp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.677C>T
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30997
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9199
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1210
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg456Trp
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

6-43039605-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039605
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039605
    reference: chr 6
allele count: 2
allele frequency: 1.954193699679512e-5
allele num: 102344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.689G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1324G>T
  hgvsp: ENSP00000418031.1:p.Gly442Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1324G>T
  hgvsp: ENSP00000340221.5:p.Gly442Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*906G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1324G>T
  hgvsp: ENSP00000377620.2:p.Gly442Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1378G>T
  hgvsp: ENSP00000259708.3:p.Gly460Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1324G>T
  hgvsp: ENSP00000377622.1:p.Gly442Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1093G>T
  hgvsp: ENSP00000395806.2:p.Gly365Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.433+248G>T
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9073
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly460Cys
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP

6-43039606-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039606
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039606
    reference: chr 6
allele count: 1
allele frequency: 9.76390868792595e-6
allele num: 102418
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.433+249G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1325G>A
  hgvsp: ENSP00000340221.5:p.Gly442Asp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1094G>A
  hgvsp: ENSP00000395806.2:p.Gly365Asp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*907G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1325G>A
  hgvsp: ENSP00000377622.1:p.Gly442Asp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1325G>A
  hgvsp: ENSP00000418031.1:p.Gly442Asp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1325G>A
  hgvsp: ENSP00000377620.2:p.Gly442Asp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.690G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1379G>A
  hgvsp: ENSP00000259708.3:p.Gly460Asp
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1094
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly460Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

6-43039608-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039608
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039608
    reference: chr 6
allele count: 2
allele frequency: 1.950800803729931e-5
allele num: 102522
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1327G>A
  hgvsp: ENSP00000418031.1:p.Gly443Arg
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1327G>A
  hgvsp: ENSP00000377622.1:p.Gly443Arg
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.692G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1381G>A
  hgvsp: ENSP00000259708.3:p.Gly461Arg
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1327G>A
  hgvsp: ENSP00000340221.5:p.Gly443Arg
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.433+251G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1327G>A
  hgvsp: ENSP00000377620.2:p.Gly443Arg
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1096G>A
  hgvsp: ENSP00000395806.2:p.Gly366Arg
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*909G>A
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8964
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31694
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 712
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly461Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

6-43039612-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039612
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039612
    reference: chr 6
allele count: 1
allele frequency: 9.742031018626763e-6
allele num: 102648
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1331C>T
  hgvsp: ENSP00000377620.2:p.Thr444Ile
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1331C>T
  hgvsp: ENSP00000340221.5:p.Thr444Ile
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1100C>T
  hgvsp: ENSP00000395806.2:p.Thr367Ile
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1385C>T
  hgvsp: ENSP00000259708.3:p.Thr462Ile
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.433+255C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*913C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1331C>T
  hgvsp: ENSP00000377622.1:p.Thr444Ile
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.696C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1331C>T
  hgvsp: ENSP00000418031.1:p.Thr444Ile
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8932
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10160
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr462Ile
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

6-43039614-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039614
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039614
    reference: chr 6
allele count: 1
allele frequency: 9.741841207988309e-6
allele num: 102650
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1333C>G
  hgvsp: ENSP00000340221.5:p.Pro445Ala
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*915C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1387C>G
  hgvsp: ENSP00000259708.3:p.Pro463Ala
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1333C>G
  hgvsp: ENSP00000418031.1:p.Pro445Ala
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.698C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.433+257C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1333C>G
  hgvsp: ENSP00000377622.1:p.Pro445Ala
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1102C>G
  hgvsp: ENSP00000395806.2:p.Pro368Ala
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1333C>G
  hgvsp: ENSP00000377620.2:p.Pro445Ala
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10265
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8937
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 937
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3446
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro463Ala
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

6-43039618-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039618
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039618
    reference: chr 6
allele count: 2
allele frequency: 1.956334611471946e-5
allele num: 102232
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1106A>G
  hgvsp: ENSP00000395806.2:p.Tyr369Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1337A>G
  hgvsp: ENSP00000418031.1:p.Tyr446Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1337A>G
  hgvsp: ENSP00000340221.5:p.Tyr446Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1337A>G
  hgvsp: ENSP00000377622.1:p.Tyr446Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.702A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1391A>G
  hgvsp: ENSP00000259708.3:p.Tyr464Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1337A>G
  hgvsp: ENSP00000377620.2:p.Tyr446Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*919A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.433+261A>G
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4913
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Tyr464Cys
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

6-43039629-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039629
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039629
    reference: chr 6
allele count: 1
allele frequency: 9.970089730807577e-6
allele num: 100300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.713G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1348G>A
  hgvsp: ENSP00000340221.5:p.Gly450Arg
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1348G>A
  hgvsp: ENSP00000377620.2:p.Gly450Arg
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1402G>A
  hgvsp: ENSP00000259708.3:p.Gly468Arg
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1348G>A
  hgvsp: ENSP00000418031.1:p.Gly450Arg
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1348G>A
  hgvsp: ENSP00000377622.1:p.Gly450Arg
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1117G>A
  hgvsp: ENSP00000395806.2:p.Gly373Arg
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-256G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*930G>A
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9973
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6635
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1248
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14032
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly468Arg
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ

6-43039631-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039631
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039631
    reference: chr 6
allele count: 1
allele frequency: 1.004116879204739e-5
allele num: 99590
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1119A>G
  hgvsp: ENST00000453940.2:c.1119A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1404A>G
  hgvsp: ENST00000259708.3:c.1404A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.715A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1350A>G
  hgvsp: ENST00000479388.1:c.1350A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1350A>G
  hgvsp: ENST00000394058.1:c.1350A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1350A>G
  hgvsp: ENST00000394056.2:c.1350A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-254A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*932A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1350A>G
  hgvsp: ENST00000347162.5:c.1350A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10245
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3238
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly468Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

6-43039632-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039632
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039632
    reference: chr 6
allele count: 1
allele frequency: 1.00357271887921e-5
allele num: 99644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1120G>A
  hgvsp: ENSP00000395806.2:p.Gly374Ser
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1351G>A
  hgvsp: ENSP00000340221.5:p.Gly451Ser
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*933G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1351G>A
  hgvsp: ENSP00000418031.1:p.Gly451Ser
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1405G>A
  hgvsp: ENSP00000259708.3:p.Gly469Ser
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1351G>A
  hgvsp: ENSP00000377620.2:p.Gly451Ser
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.716G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1351G>A
  hgvsp: ENSP00000377622.1:p.Gly451Ser
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-253G>A
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly469Ser
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

6-43039634-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039634
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039634
    reference: chr 6
allele count: 10
allele frequency: 1.008247464257627e-4
allele num: 99182
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1353C>T
  hgvsp: ENST00000394058.1:c.1353C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1122C>T
  hgvsp: ENST00000453940.2:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.718C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1353C>T
  hgvsp: ENST00000394056.2:c.1353C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-251C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1353C>T
  hgvsp: ENST00000479388.1:c.1353C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1353C>T
  hgvsp: ENST00000347162.5:c.1353C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*935C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1407C>T
  hgvsp: ENST00000259708.3:c.1407C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25704
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10110
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7560
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10454
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 588
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3200
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly469Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

6-43039655-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039655
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039655
    reference: chr 6
allele count: 1
allele frequency: 1.085446335533171e-5
allele num: 92128
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1374G>A
  hgvsp: ENST00000394056.2:c.1374G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*956G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1374G>A
  hgvsp: ENST00000394058.1:c.1374G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1143G>A
  hgvsp: ENST00000453940.2:c.1143G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1428G>A
  hgvsp: ENST00000259708.3:c.1428G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1374G>A
  hgvsp: ENST00000479388.1:c.1374G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1374G>A
  hgvsp: ENST00000347162.5:c.1374G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.739G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-230G>A
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16658
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2604
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22341
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2477
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val476Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum

6-43039665-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039665
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039665
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 88974
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*961+5G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1379+5G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1379+5G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1379+5G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1433+5G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1148+5G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-220G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1379+5G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.744+5G>C
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14133
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2240
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
hgvs: c.1433+5G>C
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-43039684-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039684
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039684
    reference: chr 6
allele count: 1
allele frequency: 1.276780470365925e-5
allele num: 78322
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1379+24C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1379+24C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*961+24C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.744+24C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1433+24C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1148+24C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1379+24C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1379+24C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-201C>G
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4561
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16098
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20325
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5980
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24503
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

6-43039690-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039690
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039690
    reference: chr 6
allele count: 2
allele frequency: 2.840666988608925e-5
allele num: 70406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1379+30C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*961+30C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-195C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1148+30C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1433+30C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1379+30C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1379+30C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1379+30C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.744+30C>G
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18436
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1232
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

6-43039690-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039690
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039690
    reference: chr 6
allele count: 48
allele frequency: 6.817600772661421e-4
allele num: 70406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.744+30C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1379+30C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1379+30C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1433+30C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1148+30C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*961+30C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1379+30C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1379+30C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-195C>T
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4005
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18226
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18436
  bin: 7.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7173
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4731
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1245
  bin: 9.75e1
  variant carriers: 51
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

6-43039693-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039693
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039693
    reference: chr 6
allele count: 2
allele frequency: 2.859921066178573e-5
allele num: 69932
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1379+33C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-192C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1379+33C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1433+33C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1379+33C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1379+33C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1148+33C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*961+33C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.744+33C>T
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18803
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6953
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18014
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3276
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1225
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5652
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

6-43039706-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039706
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039706
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 64828
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1433+46C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1148+46C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1379+46C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*961+46C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1379+46C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1379+46C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1379+46C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-179C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.744+46C>G
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 16060
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21157
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4004
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

6-43039840-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039840
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039840
    reference: chr 6
allele count: 4
allele frequency: 3.30436506625252e-5
allele num: 121052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.745-45C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*962-45C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1380-45C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-45C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1434-45C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1380-45C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1380-45C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1149-45C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1380-45C>T
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3536
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

6-43039843-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039843
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039843
    reference: chr 6
allele count: 1
allele frequency: 8.259548037531387e-6
allele num: 121072
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1149-42A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1380-42A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1380-42A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1380-42A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1434-42A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*962-42A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-42A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1380-42A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.745-42A>G
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8904
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1387
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP

6-43039849-TTCTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039849
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039845
    reference: chr 6
allele count: 1
allele frequency: 8.258183860205463e-6
allele num: 121092
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1149-32_1149-29delCTCT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1380-32_1380-29delCTCT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-32_434-29delCTCT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1380-32_1380-29delCTCT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1380-32_1380-29delCTCT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*962-32_*962-29delCTCT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.745-32_745-29delCTCT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1380-32_1380-29delCTCT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1434-32_1434-29delCTCT
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3541
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: TTCTC
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

6-43039849-TTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039849
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039847
    reference: chr 6
allele count: 1
allele frequency: 8.258183860205463e-6
allele num: 121092
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-30_434-29delCT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1380-30_1380-29delCT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1380-30_1380-29delCT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1380-30_1380-29delCT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.745-30_745-29delCT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1380-30_1380-29delCT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*962-30_*962-29delCT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1149-30_1149-29delCT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1434-30_1434-29delCT
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 32041
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: TTC
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

6-43039853-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039853
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039853
    reference: chr 6
allele count: 1
allele frequency: 8.257638315441784e-6
allele num: 121100
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-32C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*962-32C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1380-32C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1380-32C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1380-32C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1434-32C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1149-32C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.745-32C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1380-32C>G
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14703
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2968
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2395
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

6-43039855-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039855
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039855
    reference: chr 6
allele count: 1
allele frequency: 8.25695648583932e-6
allele num: 121110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1380-30C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1434-30C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*962-30C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-30C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1380-30C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1380-30C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1149-30C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.745-30C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1380-30C>T
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7755
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

6-43039863-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039863
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039862
    reference: chr 6
allele count: 10
allele frequency: 8.254094030639197e-5
allele num: 121152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*962-21delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-21delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1434-21delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1149-21delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1380-21delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1380-21delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1380-21delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1380-21delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.745-21delC
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14715
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7762
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3538
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 8.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: TC
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

6-43039865-TGG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039865
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039863
    reference: chr 6
allele count: 10
allele frequency: 8.254230293025175e-5
allele num: 121150
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1434-19_1434-18delGG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.745-19_745-18delGG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1380-19_1380-18delGG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1149-19_1149-18delGG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1380-19_1380-18delGG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1380-19_1380-18delGG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*962-19_*962-18delGG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1380-19_1380-18delGG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-19_434-18delGG
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14711
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2397
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2963
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: TGG
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

6-43039870-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039870
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039870
    reference: chr 6
allele count: 4
allele frequency: 3.300438958381465e-5
allele num: 121196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1380-15T>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*962-15T>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.745-15T>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1380-15T>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1380-15T>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1149-15T>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1434-15T>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1380-15T>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-15T>A
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2963
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

6-43039872-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039872
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039872
    reference: chr 6
allele count: 16
allele frequency: 1.32013201320132e-4
allele num: 121200
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-13T>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*962-13T>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1434-13T>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1380-13T>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.745-13T>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1149-13T>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1380-13T>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1380-13T>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1380-13T>C
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14714
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2397
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3535
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD

6-43039874-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039874
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039874
    reference: chr 6
allele count: 2
allele frequency: 1.65016501650165e-5
allele num: 121200
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1380-11T>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1380-11T>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1380-11T>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1434-11T>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-11T>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*962-11T>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1380-11T>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.745-11T>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1149-11T>A
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2396
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-43039874-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039874
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039873
    reference: chr 6
allele count: 2
allele frequency: 1.65016501650165e-5
allele num: 121200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1380-10delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1380-10delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1380-10delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1149-10delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.745-10delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1434-10delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1380-10delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*962-10delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-10delC
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: TC
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

6-43039879-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039879
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039879
    reference: chr 6
allele count: 4
allele frequency: 3.299513321785036e-5
allele num: 121230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.434-6C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.745-6C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*962-6C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1380-6C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1380-6C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1380-6C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1380-6C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1149-6C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1434-6C>T
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25520
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
hgvs: c.1434-6C>T
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

6-43039886-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039886
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039886
    reference: chr 6
allele count: 2
allele frequency: 1.649402916144356e-5
allele num: 121256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1381C>T
  hgvsp: ENSP00000377622.1:p.Pro461Ser
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.435C>T
  hgvsp: ENSP00000417620.1:p.Pro146Leu
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1381C>T
  hgvsp: ENSP00000418031.1:p.Pro461Ser
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1381C>T
  hgvsp: ENSP00000377620.2:p.Pro461Ser
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.746C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*963C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1381C>T
  hgvsp: ENSP00000340221.5:p.Pro461Ser
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1435C>T
  hgvsp: ENSP00000259708.3:p.Pro479Ser
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1150C>T
  hgvsp: ENSP00000395806.2:p.Pro384Ser
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro479Ser
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

6-43039912-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039912
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039912
    reference: chr 6
allele count: 2
allele frequency: 1.648478454386601e-5
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1461C>T
  hgvsp: ENST00000259708.3:c.1461C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*989C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.461C>T
  hgvsp: ENSP00000417620.1:p.Pro155Ser
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.772C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1407C>T
  hgvsp: ENST00000347162.5:c.1407C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1407C>T
  hgvsp: ENST00000394058.1:c.1407C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1176C>T
  hgvsp: ENST00000453940.2:c.1176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1407C>T
  hgvsp: ENST00000394056.2:c.1407C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1407C>T
  hgvsp: ENST00000479388.1:c.1407C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32539
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro155Ser
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

6-43039916-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039916
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039916
    reference: chr 6
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1411G>A
  hgvsp: ENSP00000377620.2:p.Gly471Arg
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1411G>A
  hgvsp: ENSP00000377622.1:p.Gly471Arg
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1465G>A
  hgvsp: ENSP00000259708.3:p.Gly489Arg
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.776G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1411G>A
  hgvsp: ENSP00000418031.1:p.Gly471Arg
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.465G>A
  hgvsp: ENSP00000417620.1:p.Gly156Glu
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1180G>A
  hgvsp: ENSP00000395806.2:p.Gly394Arg
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*993G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1411G>A
  hgvsp: ENSP00000340221.5:p.Gly471Arg
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14728
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2401
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32555
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly489Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

6-43039926-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039926
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039926
    reference: chr 6
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1475A>G
  hgvsp: ENSP00000259708.3:p.Tyr492Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1421A>G
  hgvsp: ENSP00000377620.2:p.Tyr474Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1421A>G
  hgvsp: ENSP00000340221.5:p.Tyr474Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.475A>G
  hgvsp: ENST00000469987.1:c.475A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1003A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1190A>G
  hgvsp: ENSP00000395806.2:p.Tyr397Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1421A>G
  hgvsp: ENSP00000377622.1:p.Tyr474Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1421A>G
  hgvsp: ENSP00000418031.1:p.Tyr474Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.786A>G
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2963
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Tyr492Cys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-43039931-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039931
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039931
    reference: chr 6
allele count: 7
allele frequency: 5.769103975736797e-5
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1480C>T
  hgvsp: ENSP00000259708.3:p.Arg494Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1426C>T
  hgvsp: ENSP00000377622.1:p.Arg476Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1195C>T
  hgvsp: ENSP00000395806.2:p.Arg399Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1008C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1426C>T
  hgvsp: ENSP00000418031.1:p.Arg476Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*2C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1426C>T
  hgvsp: ENSP00000377620.2:p.Arg476Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1426C>T
  hgvsp: ENSP00000340221.5:p.Arg476Cys
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.791C>T
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg494Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
reference allele: C
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

6-43039932-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039932
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039932
    reference: chr 6
allele count: 3
allele frequency: 2.472473132458627e-5
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1427G>A
  hgvsp: ENSP00000377622.1:p.Arg476His
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1427G>A
  hgvsp: ENSP00000418031.1:p.Arg476His
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*3G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.792G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1481G>A
  hgvsp: ENSP00000259708.3:p.Arg494His
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1427G>A
  hgvsp: ENSP00000377620.2:p.Arg476His
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1196G>A
  hgvsp: ENSP00000395806.2:p.Arg399His
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1427G>A
  hgvsp: ENSP00000340221.5:p.Arg476His
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1009G>A
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2395
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg494His
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/6-43039941-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039941
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039941
    reference: chr 6
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1436A>C
  hgvsp: ENSP00000340221.5:p.Lys479Thr
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*12A>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1436A>C
  hgvsp: ENSP00000377620.2:p.Lys479Thr
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1436A>C
  hgvsp: ENSP00000377622.1:p.Lys479Thr
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1205A>C
  hgvsp: ENSP00000395806.2:p.Lys402Thr
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1018A>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1490A>C
  hgvsp: ENSP00000259708.3:p.Lys497Thr
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1436A>C
  hgvsp: ENSP00000418031.1:p.Lys479Thr
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.801A>C
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14729
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2960
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys497Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

6-43039950-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039950
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039951
    reference: chr 6
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.811dupT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1215dupT
  hgvsp: ENSP00000395806.2:p.Ala406CysfsTer2
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1446dupT
  hgvsp: ENSP00000377620.2:p.Ala483CysfsTer2
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1500dupT
  hgvsp: ENSP00000259708.3:p.Ala501CysfsTer2
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*22dupT
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1446dupT
  hgvsp: ENSP00000340221.5:p.Ala483CysfsTer2
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1446dupT
  hgvsp: ENSP00000418031.1:p.Ala483CysfsTer2
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1446dupT
  hgvsp: ENSP00000377622.1:p.Ala483CysfsTer2
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1028dupT
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 25605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3542
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2959
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala501CysfsTer2
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

6-43039951-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039951
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039951
    reference: chr 6
allele count: 2951
allele frequency: 2.43257056185703e-2
allele num: 121312
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*22T>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1446T>C
  hgvsp: ENST00000394056.2:c.1446T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1446T>C
  hgvsp: ENST00000479388.1:c.1446T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1446T>C
  hgvsp: ENST00000347162.5:c.1446T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1446T>C
  hgvsp: ENST00000394058.1:c.1446T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1215T>C
  hgvsp: ENST00000453940.2:c.1215T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1028T>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.811T>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1500T>C
  hgvsp: ENST00000259708.3:c.1500T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.75e1
  variant carriers: 147
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 4.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 14523
  bin: 3.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 6.75e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25476
  bin: 2.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 208
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 9.75e1
  variant carriers: 988
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.25e1
  variant carriers: 186
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 187
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 8.25e1
  variant carriers: 211
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 3.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 8.75e1
  variant carriers: 200
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 4.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.25e1
  variant carriers: 211
genotype quality: GenotypeQuality
  all individuals: 1280
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8258
  bin: 9.75e1
  variant carriers: 2898
genotype quality: GenotypeQuality
  all individuals: 2907
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8883
  bin: 6.75e1
  variant carriers: 1
hgvs: p.Ala500Ala
num of homozygotes: 48
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

6-43039952-GCTGAGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039952
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039946
    reference: chr 6
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1449_1454delTGAGAC
  hgvsp: ENSP00000418031.1:p.Glu484_Thr485del
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*25_*30delTGAGAC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1449_1454delTGAGAC
  hgvsp: ENSP00000377622.1:p.Glu484_Thr485del
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1218_1223delTGAGAC
  hgvsp: ENSP00000395806.2:p.Glu407_Thr408del
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1449_1454delTGAGAC
  hgvsp: ENSP00000340221.5:p.Glu484_Thr485del
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1449_1454delTGAGAC
  hgvsp: ENSP00000377620.2:p.Glu484_Thr485del
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1503_1508delTGAGAC
  hgvsp: ENSP00000259708.3:p.Glu502_Thr503del
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.814_819delTGAGAC
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15223
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3614
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3030
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu502_Thr503del
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: GCTGAGA
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

6-43039957-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039957
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039957
    reference: chr 6
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1452G>A
  hgvsp: ENST00000347162.5:c.1452G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.817G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1221G>A
  hgvsp: ENST00000453940.2:c.1221G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1452G>A
  hgvsp: ENST00000394056.2:c.1452G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*28G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1452G>A
  hgvsp: ENST00000394058.1:c.1452G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1452G>A
  hgvsp: ENST00000479388.1:c.1452G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1506G>A
  hgvsp: ENST00000259708.3:c.1506G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1034G>A
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9330
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1039
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3611
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu502Glu
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum

6-43039957-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039957
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039957
    reference: chr 6
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1506G>C
  hgvsp: ENSP00000259708.3:p.Glu502Asp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1221G>C
  hgvsp: ENSP00000395806.2:p.Glu407Asp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*28G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1452G>C
  hgvsp: ENSP00000377622.1:p.Glu484Asp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1034G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1452G>C
  hgvsp: ENSP00000377620.2:p.Glu484Asp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1452G>C
  hgvsp: ENSP00000418031.1:p.Glu484Asp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.817G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1452G>C
  hgvsp: ENSP00000340221.5:p.Glu484Asp
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 15216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu502Asp
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-43039960-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039960
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039960
    reference: chr 6
allele count: 384
allele frequency: 3.166122489363807e-3
allele num: 121284
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1509C>T
  hgvsp: ENST00000259708.3:c.1509C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1455C>T
  hgvsp: ENST00000394056.2:c.1455C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.820C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1455C>T
  hgvsp: ENST00000347162.5:c.1455C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*31C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1037C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1455C>T
  hgvsp: ENST00000394058.1:c.1455C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1224C>T
  hgvsp: ENST00000453940.2:c.1224C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1455C>T
  hgvsp: ENST00000479388.1:c.1455C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 4722
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 4.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 26774
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15206
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 4.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2408
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr503Thr
num of homozygotes: 3
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

6-43039976-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039976
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039976
    reference: chr 6
allele count: 2
allele frequency: 1.651227687785869e-5
allele num: 121122
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.836C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1471C>T
  hgvsp: ENST00000347162.5:c.1471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1053C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*47C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1471C>T
  hgvsp: ENST00000394056.2:c.1471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1525C>T
  hgvsp: ENST00000259708.3:c.1525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1471C>T
  hgvsp: ENST00000479388.1:c.1471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1471C>T
  hgvsp: ENST00000394058.1:c.1471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1240C>T
  hgvsp: ENST00000453940.2:c.1240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: synonymous
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2409
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu509Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

6-43039976-CTGCGGTCCCGGAGACAGG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039976
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039958
    reference: chr 6
allele count: 1
allele frequency: 8.256138438929344e-6
allele num: 121122
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: splice donor
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3611
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
hgvs: c.1527_1542+2delGCGGTCCCGGAGACAGGT
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
reference allele: CTGCGGTCCCGGAGACAGG
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP

6-43039978-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039978
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039978
    reference: chr 6
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.838G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1473G>C
  hgvsp: ENST00000394058.1:c.1473G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1473G>C
  hgvsp: ENST00000394056.2:c.1473G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1242G>C
  hgvsp: ENST00000453940.2:c.1242G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1473G>C
  hgvsp: ENST00000347162.5:c.1473G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1473G>C
  hgvsp: ENST00000479388.1:c.1473G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*49G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1527G>C
  hgvsp: ENST00000259708.3:c.1527G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1055G>C
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4698
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15209
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu509Leu
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-43039978-G-GCGGTC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039978
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039983
    reference: chr 6
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: GCGGTC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1475_1479dupGGTCC
  hgvsp: ENSP00000377622.1:p.Arg494GlyfsTer36
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1475_1479dupGGTCC
  hgvsp: ENSP00000340221.5:p.Arg494GlyfsTer36
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1475_1479dupGGTCC
  hgvsp: ENSP00000377620.2:p.Arg494GlyfsTer36
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1529_1533dupGGTCC
  hgvsp: ENSP00000259708.3:p.Arg512GlyfsTer36
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1244_1248dupGGTCC
  hgvsp: ENSP00000395806.2:p.Arg417GlyfsTer36
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*51_*55dupGGTCC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1475_1479dupGGTCC
  hgvsp: ENSP00000418031.1:p.Arg494GlyfsTer36
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1057_*1061dupGGTCC
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4698
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2400
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg512GlyfsTer36
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

6-43039978-G-GCGGTCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039978
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039984
    reference: chr 6
allele count: 12
allele frequency: 9.910802775024777e-5
allele num: 121080
alternate allele: GCGGTCC
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1477_1482dupTCCCGG
  hgvsp: ENSP00000377622.1:p.Ser493_Arg494dup
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*53_*58dupTCCCGG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1477_1482dupTCCCGG
  hgvsp: ENSP00000340221.5:p.Ser493_Arg494dup
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1477_1482dupTCCCGG
  hgvsp: ENSP00000418031.1:p.Ser493_Arg494dup
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1246_1251dupTCCCGG
  hgvsp: ENSP00000395806.2:p.Ser416_Arg417dup
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1477_1482dupTCCCGG
  hgvsp: ENSP00000377620.2:p.Ser493_Arg494dup
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1531_1536dupTCCCGG
  hgvsp: ENSP00000259708.3:p.Ser511_Arg512dup
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: inframe insertion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4698
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3007
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser511_Arg512dup
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

6-43039978-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039978
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039978
    reference: chr 6
allele count: 364
allele frequency: 3.006276841757516e-3
allele num: 121080
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1242G>T
  hgvsp: ENST00000453940.2:c.1242G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*49G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1473G>T
  hgvsp: ENST00000394058.1:c.1473G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1473G>T
  hgvsp: ENST00000479388.1:c.1473G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1473G>T
  hgvsp: ENST00000347162.5:c.1473G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1527G>T
  hgvsp: ENST00000259708.3:c.1527G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.838G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1055G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1473G>T
  hgvsp: ENST00000394056.2:c.1473G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 4.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4698
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 26820
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 4.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 15209
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9262
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu509Leu
num of homozygotes: 6
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

6-43039978-GCGGTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039978
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039973
    reference: chr 6
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1475_1479delGGTCC
  hgvsp: ENSP00000377620.2:p.Arg492ProfsTer6
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1475_1479delGGTCC
  hgvsp: ENSP00000418031.1:p.Arg492ProfsTer6
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1529_1533delGGTCC
  hgvsp: ENSP00000259708.3:p.Arg510ProfsTer6
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1475_1479delGGTCC
  hgvsp: ENSP00000377622.1:p.Arg492ProfsTer6
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*51_*55delGGTCC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1475_1479delGGTCC
  hgvsp: ENSP00000340221.5:p.Arg492ProfsTer6
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1244_1248delGGTCC
  hgvsp: ENSP00000395806.2:p.Arg415ProfsTer6
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1057_*1061delGGTCC
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4698
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1320
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2400
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg510ProfsTer6
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: GCGGTC
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

6-43039979-C-CG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039979
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039980
    reference: chr 6
allele count: 2
allele frequency: 1.652537471287161e-5
allele num: 121026
alternate allele: CG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1476dupG
  hgvsp: ENSP00000340221.5:p.Ser493ValfsTer7
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1476dupG
  hgvsp: ENSP00000377622.1:p.Ser493ValfsTer7
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1245dupG
  hgvsp: ENSP00000395806.2:p.Ser416ValfsTer7
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*52dupG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1058dupG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1476dupG
  hgvsp: ENSP00000418031.1:p.Ser493ValfsTer7
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1476dupG
  hgvsp: ENSP00000377620.2:p.Ser493ValfsTer7
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1530dupG
  hgvsp: ENSP00000259708.3:p.Ser511ValfsTer7
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.839C>G
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser511ValfsTer7
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS

6-43039979-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039979
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039979
    reference: chr 6
allele count: 6
allele frequency: 4.957612413861484e-5
allele num: 121026
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1056C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*50C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1474C>T
  hgvsp: ENSP00000418031.1:p.Arg492Trp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1474C>T
  hgvsp: ENSP00000377620.2:p.Arg492Trp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1243C>T
  hgvsp: ENSP00000395806.2:p.Arg415Trp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.839C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1474C>T
  hgvsp: ENSP00000377622.1:p.Arg492Trp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1474C>T
  hgvsp: ENSP00000340221.5:p.Arg492Trp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1528C>T
  hgvsp: ENSP00000259708.3:p.Arg510Trp
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2400
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9305
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg510Trp
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

6-43039980-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039980
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039980
    reference: chr 6
allele count: 17
allele frequency: 1.404656850594087e-4
allele num: 121026
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1475G>A
  hgvsp: ENSP00000377620.2:p.Arg492Gln
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1475G>A
  hgvsp: ENSP00000418031.1:p.Arg492Gln
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1529G>A
  hgvsp: ENSP00000259708.3:p.Arg510Gln
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1057G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1475G>A
  hgvsp: ENSP00000377622.1:p.Arg492Gln
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1244G>A
  hgvsp: ENSP00000395806.2:p.Arg415Gln
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137171
  ensembl transcript: ENST00000463063
  gene symbol: KLC4
  hgvsc: ENST00000463063.1:n.840G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1475G>A
  hgvsp: ENSP00000340221.5:p.Arg492Gln
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*51G>A
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7518
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3019
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3605
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg510Gln
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

6-43039982-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039982
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039981
    reference: chr 6
allele count: 1
allele frequency: 8.265965712774223e-6
allele num: 120978
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1480delC
  hgvsp: ENSP00000418031.1:p.Arg494GlyfsTer34
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1480delC
  hgvsp: ENSP00000377622.1:p.Arg494GlyfsTer34
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1480delC
  hgvsp: ENSP00000377620.2:p.Arg494GlyfsTer34
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1480delC
  hgvsp: ENSP00000340221.5:p.Arg494GlyfsTer34
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1249delC
  hgvsp: ENSP00000395806.2:p.Arg417GlyfsTer34
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*56delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1062delC
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1534delC
  hgvsp: ENSP00000259708.3:p.Arg512GlyfsTer34
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1331
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3599
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg512GlyfsTer34
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: TC
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD

6-43039985-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039985
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039985
    reference: chr 6
allele count: 7
allele frequency: 5.789717461787865e-5
allele num: 120904
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1249C>T
  hgvsp: ENSP00000395806.2:p.Arg417Trp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*56C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1480C>T
  hgvsp: ENSP00000418031.1:p.Arg494Trp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1534C>T
  hgvsp: ENSP00000259708.3:p.Arg512Trp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1480C>T
  hgvsp: ENSP00000377622.1:p.Arg494Trp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1480C>T
  hgvsp: ENSP00000377620.2:p.Arg494Trp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1480C>T
  hgvsp: ENSP00000340221.5:p.Arg494Trp
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1062C>T
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4678
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2394
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1017
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9276
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg512Trp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP

6-43039986-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43039986
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43039986
    reference: chr 6
allele count: 15
allele frequency: 1.241043800572535e-4
allele num: 120866
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1063G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1481G>A
  hgvsp: ENSP00000418031.1:p.Arg494Gln
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1481G>A
  hgvsp: ENSP00000340221.5:p.Arg494Gln
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1481G>A
  hgvsp: ENSP00000377622.1:p.Arg494Gln
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1250G>A
  hgvsp: ENSP00000395806.2:p.Arg417Gln
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1535G>A
  hgvsp: ENSP00000259708.3:p.Arg512Gln
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*57G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1481G>A
  hgvsp: ENSP00000377620.2:p.Arg494Gln
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 26894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7473
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1322
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4996
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg512Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

6-43040039-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43040039
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43040039
    reference: chr 6
allele count: 4
allele frequency: 3.454291093110416e-5
allele num: 115798
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1070+46G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1488+46G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1542+46G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1488+46G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*64+46G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1257+46G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1488+46G>C
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1488+46G>C
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7682
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11711
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11375
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3650
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6033
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5259
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2029
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4341
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4616
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4980
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

6-43040040-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43040040
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43040040
    reference: chr 6
allele count: 1
allele frequency: 8.666712889135408e-6
allele num: 115384
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1542+47G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1488+47G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*64+47G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1070+47G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1488+47G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1257+47G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1488+47G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1488+47G>A
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11702
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5953
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12480
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5132
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5358
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4666
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4730
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2008
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum

6-43040040-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43040040
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43040040
    reference: chr 6
allele count: 2
allele frequency: 1.733342577827082e-5
allele num: 115384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1488+47G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1488+47G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1257+47G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1070+47G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1542+47G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*64+47G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1488+47G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1488+47G>T
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11747
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5953
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12480
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11702
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5132
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4666
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4730
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5358
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4034
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2525
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD

6-43040044-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43040044
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43040044
    reference: chr 6
allele count: 3
allele frequency: 2.621094569092053e-5
allele num: 114456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1488+51G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*64+51G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1542+51G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1257+51G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1488+51G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1070+51G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1488+51G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1488+51G>A
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5969
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11092
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13634
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5272
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5442
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2491
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1653
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3160
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7774
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-43040517-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43040517
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43040517
    reference: chr 6
allele count: 1
allele frequency: 8.339309838717748e-6
allele num: 119914
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1489-45G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1258-45G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1489-45G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*103G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1543-45G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1489-45G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1071-45G>A
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1489-45G>A
  variant of: http://identifiers.org/hgnc/21624
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4723
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3138
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1863
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1212
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

6-43040522-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43040522
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43040522
    reference: chr 6
allele count: 2
allele frequency: 1.666500016665e-5
allele num: 120012
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*108T>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1489-40T>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1543-40T>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1489-40T>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1258-40T>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1489-40T>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1489-40T>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1071-40T>G
  variant of: http://identifiers.org/hgnc/21624
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8481
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17205
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1150
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27015
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS

6-43040523-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43040523
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43040523
    reference: chr 6
allele count: 1
allele frequency: 8.331250520703158e-6
allele num: 120030
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1489-39A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1489-39A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*109A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1258-39A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1071-39A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1543-39A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1489-39A>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1489-39A>G
  variant of: http://identifiers.org/hgnc/21624
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3903
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8505
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8728
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1424
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 845
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1150
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

6-43040530-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43040530
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43040529
    reference: chr 6
allele count: 2
allele frequency: 1.663948883490299e-5
allele num: 120196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1489-30delG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1489-30delG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*118delG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1258-30delG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1489-30delG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1543-30delG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1071-30delG
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1489-30delG
  variant of: http://identifiers.org/hgnc/21624
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19173
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1564
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7545
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: AG
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum

6-43040539-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43040539
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43040539
    reference: chr 6
allele count: 1
allele frequency: 8.292699107705576e-6
allele num: 120588
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1543-23C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*125C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1489-23C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1489-23C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1489-23C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1258-23C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1489-23C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1071-23C>G
  variant of: http://identifiers.org/hgnc/21624
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2731
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3185
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

6-43040541-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43040541
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43040541
    reference: chr 6
allele count: 1
allele frequency: 8.288575028181154e-6
allele num: 120648
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1071-21G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1489-21G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1258-21G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1489-21G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1489-21G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*127G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1489-21G>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1543-21G>T
  variant of: http://identifiers.org/hgnc/21624
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31510
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

6-43040545-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43040545
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43040545
    reference: chr 6
allele count: 1
allele frequency: 8.283082632032337e-6
allele num: 120728
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1071-17C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1489-17C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1489-17C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1489-17C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*131C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1258-17C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1489-17C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1543-17C>T
  variant of: http://identifiers.org/hgnc/21624
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20092
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19032
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31529
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3195
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

6-43040555-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43040555
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43040555
    reference: chr 6
allele count: 2
allele frequency: 1.653220473482343e-5
allele num: 120976
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1489-7C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1489-7C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1543-7C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*141C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1258-7C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1071-7C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1489-7C>G
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1489-7C>G
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8945
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19312
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7826
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1171
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: c.1543-7C>G
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

6-43040558-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 43040558
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 43040558
    reference: chr 6
allele count: 1
allele frequency: 8.263506701703935e-6
allele num: 121014
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000395806
  ensembl transcript: ENST00000453940
  gene symbol: KLC4
  hgvsc: ENST00000453940.2:c.1258-4C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000340221
  ensembl transcript: ENST00000347162
  gene symbol: KLC4
  hgvsc: ENST00000347162.5:c.1489-4C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418031
  ensembl transcript: ENST00000479388
  gene symbol: KLC4
  hgvsc: ENST00000479388.1:c.1489-4C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000418759
  ensembl transcript: ENST00000467906
  gene symbol: KLC4
  hgvsc: ENST00000467906.1:c.*1071-4C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377622
  ensembl transcript: ENST00000394058
  gene symbol: KLC4
  hgvsc: ENST00000394058.1:c.1489-4C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000377620
  ensembl transcript: ENST00000394056
  gene symbol: KLC4
  hgvsc: ENST00000394056.2:c.1489-4C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000259708
  ensembl transcript: ENST00000259708
  gene symbol: KLC4
  hgvsc: ENST00000259708.3:c.1543-4C>T
  variant of: http://identifiers.org/hgnc/21624
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137171
  ensembl protein: ENSP00000417620
  ensembl transcript: ENST00000469987
  gene symbol: KLC4
  hgvsc: ENST00000469987.1:c.*144C>T
  variant of: http://identifiers.org/hgnc/21624
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8971
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32522
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: c.1543-4C>T
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 36498
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1273
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11546
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1322
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3329
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4716
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 6.345177664974619e-4
allele num: 7880
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7182
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.099868015838099e-4
allele num: 9092
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.457216940363008e-5
allele num: 57850
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13158
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.088e1

DP
type: SiteQuality
SIO_000300: 1.239602e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

GenotypeQuality
all individuals: 752
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1112
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1041
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37581
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10968
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1203
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 449
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3437
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.405414609228674e-5
allele num: 58730
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4788
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13264
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.217e0

QD
type: SiteQuality
SIO_000300: 1.031e1

VQSLOD
type: SiteQuality
SIO_000300: -6.94e-2

FS
type: SiteQuality
SIO_000300: 1.756e0

MQ
type: SiteQuality
SIO_000300: 5.891e1

DP
type: SiteQuality
SIO_000300: 1.260171e6

GenotypeQuality
all individuals: 186
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 160
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10963
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3444
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37625
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4796
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.700738120344229e-5
allele num: 58798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8282
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13266
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9204
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.06e-1

FS
type: SiteQuality
SIO_000300: 2.845e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.639e-1

DP
type: SiteQuality
SIO_000300: 1.261147e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.271e0

MQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

QD
type: SiteQuality
SIO_000300: 1.843e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 10946
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37836
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1058
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3442
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7364
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13266
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9204
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8308
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.398355196085095e-5
allele num: 58852
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e-1

FS
type: SiteQuality
SIO_000300: 2.071e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.786e0

VQSLOD
type: SiteQuality
SIO_000300: 1.11e-1

DP
type: SiteQuality
SIO_000300: 1.264209e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

QD
type: SiteQuality
SIO_000300: 2.217e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e-1

GenotypeQuality
all individuals: 386
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 696
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11105
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 234
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37756
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3454
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8354
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13292
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.69848495142333e-5
allele num: 58876
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4816
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.609e0

MQRankSum
type: SiteQuality
SIO_000300: -7.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.766e0

DP
type: SiteQuality
SIO_000300: 1.264728e6

VQSLOD
type: SiteQuality
SIO_000300: -1.497e0

QD
type: SiteQuality
SIO_000300: 6.37e0

FS
type: SiteQuality
SIO_000300: 6.064e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.03e0

GenotypeQuality
all individuals: 1054
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11233
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37711
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 178
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9200
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13298
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.698254194687861e-5
allele num: 58884
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4806
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.04e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.319e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

DP
type: SiteQuality
SIO_000300: 1.265036e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.37e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

MQ
type: SiteQuality
SIO_000300: 5.756e1

GenotypeQuality
all individuals: 879
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3378
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11861
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1119
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36556
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 207
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7352
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4780
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.177700348432056e-4
allele num: 9184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8298
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13294
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.258029e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.77e0

QD
type: SiteQuality
SIO_000300: 1.23e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 8.75e1
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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: 468
bin: 4.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 706
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.735809755250825e-5
allele num: 57610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4658
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7960
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9042
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7200
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13124
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.09e-1

QD
type: SiteQuality
SIO_000300: 8.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

FS
type: SiteQuality
SIO_000300: 1.44e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.4e-1

DP
type: SiteQuality
SIO_000300: 1.224602e6

MQ
type: SiteQuality
SIO_000300: 5.942e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4624
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.656967840735069e-5
allele num: 13060
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7822
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8992
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57242
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e-1

QD
type: SiteQuality
SIO_000300: 1.14e1

MQ
type: SiteQuality
SIO_000300: 5.898e1

DP
type: SiteQuality
SIO_000300: 1.212878e6

FS
type: SiteQuality
SIO_000300: 2.273e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

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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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.64642911760208e-5
allele num: 13078
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57272
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7154
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4620
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -5.412e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.212582e6

QD
type: SiteQuality
SIO_000300: 8.859999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

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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variant carriers: 10

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1350
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GenotypeQuality
all individuals: 153
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 10
allele frequency: 1.292657704239917e-3
allele num: 7736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13038
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8968
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7120
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 698
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57018
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-1

QD
type: SiteQuality
SIO_000300: 9.9e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.52e-1

DP
type: SiteQuality
SIO_000300: 1.204935e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.107e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.48e-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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bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6644
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6646
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52894
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.170411985018727e-4
allele num: 8544
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.275e0

MQRankSum
type: SiteQuality
SIO_000300: -1.448e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.37e-1

DP
type: SiteQuality
SIO_000300: 1.074612e6

VQSLOD
type: SiteQuality
SIO_000300: -4.407e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.377e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.53e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1939
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variant carriers: 0

GenotypeQuality
all individuals: 1227
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6218
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12358
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3992
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-3

DP
type: SiteQuality
SIO_000300: 1.018062e6

MQRankSum
type: SiteQuality
SIO_000300: -1.652e0

MQ
type: SiteQuality
SIO_000300: 5.766e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.06e0

VQSLOD
type: SiteQuality
SIO_000300: -2.157e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.225981657911139e-5
allele num: 44924
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3318
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4660
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11644
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.18e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.359e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.29e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
type: SiteQuality
SIO_000300: 5.71e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.887e0

DP
type: SiteQuality
SIO_000300: 8.62901e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.932e0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 821
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4912
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2888
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.796945193171608e-4
allele num: 11130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3552
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.24e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.42e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.95e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.11726e5

QD
type: SiteQuality
SIO_000300: 1.43e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20469
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1232
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5437
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 170
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 488
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2909
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3002
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5030
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 438
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 298
bin: 8.25e1
variant carriers: 1

African
type: Population
allele count: 46
allele frequency: 6.469760900140647e-3
allele num: 7110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4912
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.984725965858041e-5
allele num: 11130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.48003571251426e-5
allele num: 40322
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.42e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.24e0

QD
type: SiteQuality
SIO_000300: 1.43e1

VQSLOD
type: SiteQuality
SIO_000300: 5.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

DP
type: SiteQuality
SIO_000300: 8.11726e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

GenotypeQuality
all individuals: 2929
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7069
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 815
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21744
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5321
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4668
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2852
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1198
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2870
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4882
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7088
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11074
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.001250312578144e-5
allele num: 39990
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.361e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.07122e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.66e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

QD
type: SiteQuality
SIO_000300: 1.795e1

GenotypeQuality
all individuals: 140
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18332
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5225
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1201
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4635
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1358
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7516
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3308
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5554
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3537
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4424
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2946
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36780
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6748
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2700
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10770
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.012e1

VQSLOD
type: SiteQuality
SIO_000300: 2.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

DP
type: SiteQuality
SIO_000300: 7.76044e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.86e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31598
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2955
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7751
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 171
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 184
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2389
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8872
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1050
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.003482019571351e-5
allele num: 66628
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.72e-1

FS
type: SiteQuality
SIO_000300: 1.557e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.75e0

MQRankSum
type: SiteQuality
SIO_000300: -1.64e-1

DP
type: SiteQuality
SIO_000300: 1.95476e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e0

QD
type: SiteQuality
SIO_000300: 4.0e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.661e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 2391
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 73
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31805
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3533
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7754
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 182
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2953
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.773260359655981e-5
allele num: 10232
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e0

MQRankSum
type: SiteQuality
SIO_000300: -5.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

QD
type: SiteQuality
SIO_000300: 1.563e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e-2

FS
type: SiteQuality
SIO_000300: 6.066e0

MQ
type: SiteQuality
SIO_000300: 5.913e1

VQSLOD
type: SiteQuality
SIO_000300: -4.606e-1

DP
type: SiteQuality
SIO_000300: 1.955718e6

GenotypeQuality
all individuals: 122
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32041
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8907
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7756
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1383
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2970
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2392
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.97e-1

MQ
type: SiteQuality
SIO_000300: 6.018e1

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

FS
type: SiteQuality
SIO_000300: 1.1675e1

QD
type: SiteQuality
SIO_000300: 1.561e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

DP
type: SiteQuality
SIO_000300: 1.957634e6

GenotypeQuality
all individuals: 2392
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2970
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8907
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7756
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1383
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3541
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500330072615976e-5
allele num: 66652
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQ
type: SiteQuality
SIO_000300: 6.018e1

VQSLOD
type: SiteQuality
SIO_000300: 4.97e-1

FS
type: SiteQuality
SIO_000300: 1.1675e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

DP
type: SiteQuality
SIO_000300: 1.957634e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.34e-1

QD
type: SiteQuality
SIO_000300: 1.561e1

GenotypeQuality
all individuals: 89
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3540
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7757
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 32095
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8901
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1382
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10242
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.53e-1

FS
type: SiteQuality
SIO_000300: 2.637e0

QD
type: SiteQuality
SIO_000300: 1.493e1

MQRankSum
type: SiteQuality
SIO_000300: 5.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e0

MQ
type: SiteQuality
SIO_000300: 5.836e1

DP
type: SiteQuality
SIO_000300: 1.958493e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.401e0

VQSLOD
type: SiteQuality
SIO_000300: -2.768e0

GenotypeQuality
all individuals: 8902
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2967
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1383
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32173
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2399
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3539
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1058
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10244
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.493e0

QD
type: SiteQuality
SIO_000300: 1.48e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.03e-1

DP
type: SiteQuality
SIO_000300: 1.958979e6

FS
type: SiteQuality
SIO_000300: 1.715e0

MQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

GenotypeQuality
all individuals: 67
bin: 3.25e1
variant carriers: 1

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

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32291
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

African
type: Population
allele count: 9
allele frequency: 8.773640085786703e-4
allele num: 10258
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.42e-1

QD
type: SiteQuality
SIO_000300: 1.104e1

MQRankSum
type: SiteQuality
SIO_000300: -1.684e0

FS
type: SiteQuality
SIO_000300: 2.503e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.275e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.37e-1

MQ
type: SiteQuality
SIO_000300: 5.658e1

DP
type: SiteQuality
SIO_000300: 1.960406e6

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 8921
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variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 8.777062609713282e-4
allele num: 10254
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.601e1

FS
type: SiteQuality
SIO_000300: 2.416e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.649e0

MQRankSum
type: SiteQuality
SIO_000300: -2.049e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.399999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.961065e6

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.046e1

GenotypeQuality
all individuals: 7751
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1060
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8934
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.498695378340282e-5
allele num: 66686
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.721952167995334e-5
allele num: 10286
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -8.72e-1

QD
type: SiteQuality
SIO_000300: 1.487e1

DP
type: SiteQuality
SIO_000300: 1.961038e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.41e-1

FS
type: SiteQuality
SIO_000300: 9.350000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-1

GenotypeQuality
all individuals: 32402
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 16

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 2963
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.399160293897136e-4
allele num: 66690
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.6e0

DP
type: SiteQuality
SIO_000300: 1.961753e6

FS
type: SiteQuality
SIO_000300: 6.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

QD
type: SiteQuality
SIO_000300: 1.388e1

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

GenotypeQuality
all individuals: 7737
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2
bin: 1.75e1
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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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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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
all individuals: 10
bin: 4.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999040307101727e-5
allele num: 66688
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.960825e6

MQ
type: SiteQuality
SIO_000300: 5.933e1

FS
type: SiteQuality
SIO_000300: 2.058e0

QD
type: SiteQuality
SIO_000300: 1.42e1

MQRankSum
type: SiteQuality
SIO_000300: -4.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 11
bin: 5.75e1
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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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2963
bin: 7.25e1
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GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999040307101727e-5
allele num: 66688
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -7.57e-1

FS
type: SiteQuality
SIO_000300: 2.058e0

DP
type: SiteQuality
SIO_000300: 1.960825e6

VQSLOD
type: SiteQuality
SIO_000300: 3.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.45e-1

QD
type: SiteQuality
SIO_000300: 1.42e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2395
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.99868058054456e-5
allele num: 66696
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-1

DP
type: SiteQuality
SIO_000300: 1.961438e6

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.896e1

MQRankSum
type: SiteQuality
SIO_000300: -1.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.62e-1

FS
type: SiteQuality
SIO_000300: 5.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.569e0

GenotypeQuality
all individuals: 32483
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 8945
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998320940273447e-5
allele num: 66704
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.966e1

InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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FS
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MQRankSum
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QD
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ClippingRankSum
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DP
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

South Asian
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allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
type: SiteQuality
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 6.0e1

DP
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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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

South Asian
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allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

MQRankSum
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MQ
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BaseQRankSum
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FS
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QD
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InbreedingCoeff
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SIO_000300: -1.0e-4

DP
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ClippingRankSum
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

South Asian
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allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.919e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.63e-1

MQRankSum
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DP
type: SiteQuality
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QD
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FS
type: SiteQuality
SIO_000300: 3.2e0

BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.3e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5
allele frequency: 7.494903465643362e-5
allele num: 66712
num of homozygotes: 0

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

South Asian
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allele count: 2
allele frequency: 1.211680600993578e-4
allele num: 16506
num of homozygotes: 0

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

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

Latino
type: Population
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allele frequency: 0.0e0
allele num: 11574
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DP
type: SiteQuality
SIO_000300: 1.963404e6

FS
type: SiteQuality
SIO_000300: 1.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.79e-1

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e-2

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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variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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South Asian
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allele num: 16506
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QD
type: SiteQuality
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ClippingRankSum
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FS
type: SiteQuality
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ReadPosRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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MQRankSum
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VQSLOD
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MQ
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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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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
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South Asian
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Latino
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East Asian
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African
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allele frequency: 9.619084263178146e-5
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European (Non-Finnish)
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allele count: 0
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allele num: 66698
num of homozygotes: 0

FS
type: SiteQuality
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VQSLOD
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MQ
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DP
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ReadPosRankSum
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MQRankSum
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QD
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 904
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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South Asian
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Latino
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East Asian
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BaseQRankSum
type: SiteQuality
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DP
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.022e1

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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East Asian
type: Population
allele count: 155
allele frequency: 1.793981481481481e-2
allele num: 8640
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Other
type: Population
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South Asian
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allele count: 474
allele frequency: 2.871335110249576e-2
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Latino
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allele frequency: 7.089745806674736e-3
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1934
allele frequency: 2.900158953903368e-2
allele num: 66686
num of homozygotes: 35

African
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allele count: 91
allele frequency: 8.753366679492112e-3
allele num: 10396
num of homozygotes: 0

European (Finnish)
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allele count: 192
allele frequency: 2.903811252268602e-2
allele num: 6612
num of homozygotes: 1

DP
type: SiteQuality
SIO_000300: 2.056128e6

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.254e0

ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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SIO_000300: 1.233e1

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.92e-1

GenotypeQuality
all individuals: 1342
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9334
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1039
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.87e-1

FS
type: SiteQuality
SIO_000300: 4.384e0

MQRankSum
type: SiteQuality
SIO_000300: -4.085e0

MQ
type: SiteQuality
SIO_000300: 4.612e1

QD
type: SiteQuality
SIO_000300: 1.094e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.26e-1

DP
type: SiteQuality
SIO_000300: 1.891136e6

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 5582
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -3.565e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.258e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.9e-2

DP
type: SiteQuality
SIO_000300: 1.890755e6

FS
type: SiteQuality
SIO_000300: 1.7235e1

MQRankSum
type: SiteQuality
SIO_000300: -1.506e0

GenotypeQuality
all individuals: 2416
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5582
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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
all individuals: 9330
bin: 6.75e1
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GenotypeQuality
all individuals: 1341
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66674
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e0

VQSLOD
type: SiteQuality
SIO_000300: -3.565e0

QD
type: SiteQuality
SIO_000300: 1.258e1

DP
type: SiteQuality
SIO_000300: 1.890755e6

FS
type: SiteQuality
SIO_000300: 1.7235e1

MQRankSum
type: SiteQuality
SIO_000300: -1.506e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.97e-1

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 3607
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 16
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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: 13
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variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 1026
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 5649
bin: 9.75e1
variant carriers: 381

GenotypeQuality
all individuals: 1332
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 347
allele frequency: 3.338464498749279e-2
allele num: 10394
num of homozygotes: 3

South Asian
type: Population
allele count: 2
allele frequency: 1.212121212121212e-4
allele num: 16500
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.649917504124794e-4
allele num: 66670
num of homozygotes: 0

Latino
type: Population
allele count: 23
allele frequency: 1.988243430152144e-3
allele num: 11568
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.03e-2

QD
type: SiteQuality
SIO_000300: 1.238e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.465e0

DP
type: SiteQuality
SIO_000300: 1.898199e6

VQSLOD
type: SiteQuality
SIO_000300: 4.81e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

FS
type: SiteQuality
SIO_000300: 1.358e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-2

GenotypeQuality
all individuals: 9275
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 55
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GenotypeQuality
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GenotypeQuality
all individuals: 38
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GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 299
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 5301
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 34151
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3013
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.89e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.366e0

QD
type: SiteQuality
SIO_000300: 5.19e0

FS
type: SiteQuality
SIO_000300: 7.216e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.25e-1

DP
type: SiteQuality
SIO_000300: 1.877155e6

VQSLOD
type: SiteQuality
SIO_000300: 8.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.397e0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5301
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3013
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 34
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 299
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variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 2409
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variant carriers: 0

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 9275
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1336
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.366e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.934e1

MQRankSum
type: SiteQuality
SIO_000300: 1.89e-1

QD
type: SiteQuality
SIO_000300: 5.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.397e0

FS
type: SiteQuality
SIO_000300: 7.216e0

DP
type: SiteQuality
SIO_000300: 1.877155e6

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5385
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GenotypeQuality
all individuals: 2400
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GenotypeQuality
all individuals: 60
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 34075
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66512
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

QD
type: SiteQuality
SIO_000300: 1.397e1

MQ
type: SiteQuality
SIO_000300: 5.977e1

FS
type: SiteQuality
SIO_000300: 1.543e0

DP
type: SiteQuality
SIO_000300: 1.879911e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.879e0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 58
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
all individuals: 30
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34075
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3007
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503488092374308e-5
allele num: 66512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.879e0

QD
type: SiteQuality
SIO_000300: 1.397e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-2

MQ
type: SiteQuality
SIO_000300: 5.977e1

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e-1

FS
type: SiteQuality
SIO_000300: 1.543e0

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

DP
type: SiteQuality
SIO_000300: 1.879911e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.07e-1

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
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GenotypeQuality
all individuals: 9262
bin: 6.75e1
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GenotypeQuality
all individuals: 1320
bin: 9.25e1
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GenotypeQuality
all individuals: 339
bin: 2.25e1
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GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 12

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.635767970707265e-5
allele num: 10378
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158748551564311e-4
allele num: 8630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.020928554245851e-5
allele num: 66512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.425418384671356e-4
allele num: 16492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

QD
type: SiteQuality
SIO_000300: 1.397e1

DP
type: SiteQuality
SIO_000300: 1.879911e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

FS
type: SiteQuality
SIO_000300: 1.543e0

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.879e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-2

GenotypeQuality
all individuals: 2400
bin: 8.25e1
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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bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513775355737209e-4
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 29
allele frequency: 4.360115467885494e-4
allele num: 66512
num of homozygotes: 0

African
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allele count: 311
allele frequency: 2.99672383888996e-2
allele num: 10378
num of homozygotes: 6

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

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

Latino
type: Population
allele count: 22
allele frequency: 1.903114186851211e-3
allele num: 11560
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.543e0

DP
type: SiteQuality
SIO_000300: 1.879911e6

QD
type: SiteQuality
SIO_000300: 1.397e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.879e0

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

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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bin: 5.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503488092374308e-5
allele num: 66512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.977e1

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

FS
type: SiteQuality
SIO_000300: 1.543e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e-1

QD
type: SiteQuality
SIO_000300: 1.397e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.879e0

DP
type: SiteQuality
SIO_000300: 1.879911e6

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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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.008604609182261e-5
allele num: 66476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.29e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.09e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
type: SiteQuality
SIO_000300: 1.866234e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

FS
type: SiteQuality
SIO_000300: 1.843e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.025813827546783e-5
allele num: 66476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 1.866234e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

FS
type: SiteQuality
SIO_000300: 1.843e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

VQSLOD
type: SiteQuality
SIO_000300: 2.2e0

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-2

QD
type: SiteQuality
SIO_000300: 1.29e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-1

GenotypeQuality
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variant carriers: 17

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 2.557236980655254e-4
allele num: 66478
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.417e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.01e-1

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -5.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.8e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.4e-1

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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bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
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South Asian
type: Population
allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66446
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.68e-1

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.031e1

VQSLOD
type: SiteQuality
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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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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.024640780793445e-5
allele num: 66394
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.599653379549393e-4
allele num: 11540
num of homozygotes: 0

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

African
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MQRankSum
type: SiteQuality
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VQSLOD
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ClippingRankSum
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MQ
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FS
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.213150551983501e-4
allele num: 16486
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 1.039861351819757e-3
allele num: 11540
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506750241080039e-5
allele num: 66368
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

FS
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.331e1

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 1.858639e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.5e0

GenotypeQuality
all individuals: 4829
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2829
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2516
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4283
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13923
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2049
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2746
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1233
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1876
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7964
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11014
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63194
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.005607850991388e-4
allele num: 9986
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.817e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.94e0

DP
type: SiteQuality
SIO_000300: 1.536378e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

QD
type: SiteQuality
SIO_000300: 1.23e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.398e0

GenotypeQuality
all individuals: 715
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2044
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11670
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2901
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2718
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4828
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2525
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4034
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.588865232450984e-5
allele num: 62938
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16240
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9946
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7920
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10960
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.17e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.21e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

VQSLOD
type: SiteQuality
SIO_000300: 7.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.528211e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.54e-1

GenotypeQuality
all individuals: 2901
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2044
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3019
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1235
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2008
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variant carriers: 0

GenotypeQuality
all individuals: 11670
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4828
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 535
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9946
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62938
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7920
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10960
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.231527093596059e-4
allele num: 16240
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.7e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.54e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.21e-1

DP
type: SiteQuality
SIO_000300: 1.528211e6

QD
type: SiteQuality
SIO_000300: 1.17e1

GenotypeQuality
all individuals: 2688
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2033
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1953
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variant carriers: 0

GenotypeQuality
all individuals: 602
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variant carriers: 0

GenotypeQuality
all individuals: 5823
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 903
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variant carriers: 0

GenotypeQuality
all individuals: 4827
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3537
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variant carriers: 0

GenotypeQuality
all individuals: 4417
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1233
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4708
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62326
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6484
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10858
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.030915336431602e-4
allele num: 9898
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.603e0

FS
type: SiteQuality
SIO_000300: 1.535e0

DP
type: SiteQuality
SIO_000300: 1.518347e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.48e-1

QD
type: SiteQuality
SIO_000300: 1.156e1

MQ
type: SiteQuality
SIO_000300: 5.903e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

GenotypeQuality
all individuals: 43
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1401
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1135
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1317
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2130
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
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variant carriers: 0

GenotypeQuality
all individuals: 2667
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7253
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23854
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8721
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512355948095944e-5
allele num: 66122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16058
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.382e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

QD
type: SiteQuality
SIO_000300: 7.7e0

FS
type: SiteQuality
SIO_000300: 8.451000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.758547e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2129
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7394
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variant carriers: 0

GenotypeQuality
all individuals: 1169
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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GenotypeQuality
all individuals: 34
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GenotypeQuality
all individuals: 2665
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variant carriers: 0

GenotypeQuality
all individuals: 3127
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variant carriers: 0

GenotypeQuality
all individuals: 8727
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1139
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 612
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variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16070
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66158
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.745505323791238e-4
allele num: 11458
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.13e-1

QD
type: SiteQuality
SIO_000300: 9.390000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

MQRankSum
type: SiteQuality
SIO_000300: -1.65e-1

DP
type: SiteQuality
SIO_000300: 1.774549e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1554
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 624
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variant carriers: 0

GenotypeQuality
all individuals: 619
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variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3137
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.223549912870301e-5
allele num: 16068
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66172
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.926e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

DP
type: SiteQuality
SIO_000300: 1.777815e6

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

VQSLOD
type: SiteQuality
SIO_000300: -2.161e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.17e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 15
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 371
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GenotypeQuality
all individuals: 29340
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.718395815170009e-5
allele num: 11470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509479531457553e-5
allele num: 66248
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.463e1

FS
type: SiteQuality
SIO_000300: 2.173e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.798983e6

MQ
type: SiteQuality
SIO_000300: 6.049e1

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

GenotypeQuality
all individuals: 7705
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8757
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GenotypeQuality
all individuals: 31211
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GenotypeQuality
all individuals: 181
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GenotypeQuality
all individuals: 506
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GenotypeQuality
all individuals: 420
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GenotypeQuality
all individuals: 1577
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variant carriers: 0

GenotypeQuality
all individuals: 155
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GenotypeQuality
all individuals: 2172
bin: 8.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66414
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.161170459823502e-4
allele num: 8612
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.631e-1

DP
type: SiteQuality
SIO_000300: 1.819697e6

QD
type: SiteQuality
SIO_000300: 1.097e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 9.159000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.666e0

MQRankSum
type: SiteQuality
SIO_000300: -8.159999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.5e-1

GenotypeQuality
all individuals: 159
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1166
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8757
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1575
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3197
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2740
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7746
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.686587908269631e-5
allele num: 11512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16226
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.313e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.77e0

MQRankSum
type: SiteQuality
SIO_000300: 5.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.75e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.822799e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.857e0

GenotypeQuality
all individuals: 300
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2758
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7756
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1576
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8756
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1169
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.635767970707265e-5
allele num: 10378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66462
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

DP
type: SiteQuality
SIO_000300: 1.827986e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

FS
type: SiteQuality
SIO_000300: 1.592e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.12e-1

QD
type: SiteQuality
SIO_000300: 1.082e1

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3205
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8766
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 2179
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2790
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1578
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32440
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16354
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.005801196308876e-5
allele num: 66538
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.322e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

QD
type: SiteQuality
SIO_000300: 1.159e1

FS
type: SiteQuality
SIO_000300: 3.492e0

DP
type: SiteQuality
SIO_000300: 1.836488e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
all individuals: 2795
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7835
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 236
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0